Petitioner: AGENCY FOR HEALTH CARE ADMINISTRATION
Respondent: SENIOR LIFESTYLES, LLC, D/B/A KIPLING MANOR RETIREMENT CENTER
Judges: ROBERT S. COHEN
Agency: Agency for Health Care Administration
Locations: Pensacola, Florida
Filed: Oct. 28, 2008
Status: Closed
Settled and/or Dismissed prior to entry of RO/FO on Monday, February 9, 2009.
Latest Update: Dec. 22, 2024
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STATE OF FLORIDA > a
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AGENCY FOR HEALTH CARE ADMINISTRATION OL), by &
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STATE OF FLORIDA AGENCY FOR EB oe,
HEALTH CARE ADMINISTRATION, Wy e
SF den
Petitioner,
Case Nos. 2008010733
vs. 2008010608
KIPLING MANOR RETIREMENT CENTER,
Respondent.
/
ADMINISTRATIVE COMPLAINT
COMES NOW the Agency for Health Care Administration (hereinafter “Agency”), by
and through the undersigned counsel, and files this Administrative Complaint against KIPLING
MANOR RETIREMENT CENTER, (hereinafter “Respondent”), pursuant to Section 120.569,
and 120.57, Florida Statutes, (2007), and alleges:
NATURE OF THE ACTION
This is an action to revoke the Respondent’s license to operate an assisted living facility
and impose an administrative fine in the sum of thirty-seven thousand dollars ($37,000.00) based
upon five (5) State Class I deficiencies (Counts I, II, If], VI, VID), two (2) State Class I
deficiencies (Count IV, VIII), one State Class II deficiency (Count IX), one State Class II
deficiency (Count V), and in addition an action to impose an survey fee in the sum of five
hundred dollars ($500.00) pursuant to §429.275.
JURISDICTION AND VENUE
1. The Agency has jurisdiction pursuant to §§ 20.42, 120.60 and 400.407, Florida Statutes
(2007).
2. Venue lies pursuant to Florida Administrative Code R. 28-106.207.
PARTIES |
3. The Agency is the regulatory authority responsible for licensure of assisted living
facilities and enforcement of all applicable federal regulations, state statutes and rules governing
assisted living facilities pursuant to the Chapter 429, Part I, Florida Statutes, and Chapter 58A-5,
Florida Administrative Code, respectively.
4. Respondent operates a sixty five (65)-bed assisted living facility located at 7901 Kipling
Street, Pensacola, Florida 32514, and is licensed as an assisted living facility, under license
number 7285.
5. Respondent was at all times material hereto a licensed facility under the licensing
authority of the Agency, and was required to comply with all applicable rules and statutes.
COUNT I
Respondent’s administrator failed to ensure adequate care to all residents as evidenced by
failing to provide assistance with self administration of medications and had unlicensed
staff administer medications (A610); facility failed to have a licensed nurse administer
medications and facility failed to administer psychiatric medications in accordance with the
physician orders (A613); facility failed to maintain an accurate medication observation
record (A615); facility failed to store medications in a locked cart out of reach of
wandering and confused residents on the specialty unit (A619); facility failed to ensure that
prescriptions were filled in a timely manner (A631); facility failed to notify family,
physician, or responsible party of resident changes in condition (A706); facility failed to
serve diets as ordered by the physician, failed to follow the menu, and failed to have
therapeutic meals listed on menus (A806).
6. The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
7. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
8. Based on observation, interview and record review, Respondent’s administrator failed to
ensure adequate care to all residents as evidenced by facility failing to provide assistance with
self administration of medications and had unlicensed staff administer medications (A610);
facility failed to have a licensed nurse administer medications and facility failed to administer
psychiatric medications in accordance with the physician orders (A613); facility failed to
maintain an accurate medication observation record (A615); facility failed to store medications
in a locked cart out of reach of wandering and confused residents on the specialty unit (A619);
facility failed to ensure that prescriptions were filled in a timely manner (A631); facility failed to
notify family, physician, or responsible party of resident changes in condition (A706); facility
failed to serve diets as ordered by the physician, failed to follow the menu, and failed to have
therapeutic meals listed on menus(A806), the same being in violation of law.
9. That the failure of Respondent’s administrator to ensure adequate care to all residents as
evidenced by the facility failing to provide assistance with self administration of medications and
having unlicensed staff administer medications (A610); facility failed to have a licensed nurse |
administer medications and facility failed to administer psychiatric medications in accordance
with the physician orders (A613); facility failed to maintain an accurate medication observation
record (A615); facility failed to store medications in a locked cart out of reach of wandering and
confused residents on the specialty unit (A619); facility failed to ensure that prescriptions were
filled in a timely manner (A631); facility failed to notify family, physician, or responsible party
of resident changes in condition (A706); facility failed to serve diets as ordered by the physician,
failed to follow the menu, and failed to have therapeutic meals listed on menus (A806), the same
being in violation of law.
10. That the Agency determined that this deficient practice presented an imminent danger to
the residents and serious physical or emotional harm would result and cited Respondent for a
State Class I deficiency.
11. The regulatory provisions of the Fla. Admin. Code (2007) that are pertinent to this
alleged violation read as follows:
58A-5.019 (1) Staffing Standards.
ADMINISTRATORS. Every facility shall be under the supervision of an
administrator who is responsible for the operation and maintenance of the facility
including the management of all staff and the provision of adequate care to all
residents as required by Part I of Chapter 429, F.S., and this rule chapter.
* OK OK
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$5,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to 58A-
5.019(1) Fla. Admin. Code (2007).
COUNT II
Respondent failed to provide assistance with self administration, and had unlicensed staff
administer medications to 4 of 4 residents (#1, 2, 8, 9) during medication pass observation.
Medication pass observation was observed on all units (2 of 2) and 2 medication technicians
(med techs) were observed.
12. The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
13. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
14. That based on observation, staff interview, and record review, the Respondent has failed
to provide assistance with self administration, and had unlicensed staff administer medications to
4 of 4 residents (#1, 2, 8, 9) during medication pass observation. Medication pass observation
4
was observed on all units (2 of 2) and 2 medication technicians (med techs) were observed, the
same being in violation of law. The findings include:
a.
Observation of medication pass on the special care unit on 9/3/08 at 8:40 AM
revealed a med tech standing at the medication cart (alone) placing
medications in a cup for resident #2: Roxanol (narcotic analgesic) 5 mg,
Glipizide (antidiabetic agent) 5 mg , Lasix (diuretic) 20 mg, Zoloft
(antidepressant) 100 mg, K+ 10 meq (potassium), Risperdal (antipsychotic
agent) 0.5 mg, Trilisate (arthritis) 500 mg, Tylenol (analgesic) 500 mg,
Valium (anxiety disorders) 2 mg. The medications were placed in a
medication cup and crushed except Roxanol was added to 8 ounces of orange
juice (OJ). The medications were taken to the resident at the breakfast table in
the common dining room.
. The med tech did not take the medication, in its dispensed, properly labeled
container, from where it was stored and bring it to the resident. The med tech
did not, in the presence of the resident, read the label, open the container,
remove the prescribed amount of medication from the container, and close the
container.
The med tech poured the crushed medications on the top of the resident’s
pancakes and placed the OJ with the Roxanol at the residents place. The med
tech stated she has to feed the resident and this is the only way they can get
the resident to take the medication.. The med tech was busy with other things
and left the resident sitting at the dining room table with the crushed
medications on top of the pancakes and the OJ with the Roxanol on the table.
There were two other residents sitting at the dining room table with resident
#2 at this time. Both residents were confused and wandered. These three
residents were not supervised or observed by the medication tech. Resident #2
ate half of the food and drank half of the OJ. Resident #2 did not receive
Natural Tears one gtt (drop) in both eyes as ordered. The med tech stated the
medication was not available from the pharmacy.
. Observation of medication pass on the special care unit on 9/3/08 at 8:15 AM
revealed a med tech aide standing at the medication cart alone placing the
following medications for resident #1 in a medication cup: Cogentin
(antiparkinson's disease) one 20 milligrams (mg) and one Mestinon
(myasthenia gravis) 60 mg. The medications were placed in a medication cup
at the cart then taken in the cup to the resident, The medication was poured
on to the bed and the resident picked the medication up and took the
medication. The med tech did not, take the medication, in its dispensed,
properly labeled container, from where it was stored and bring it to the
resident. The med tech did not, in the presence of the resident, read the label,
open the container, remove the prescribed amount of medication from the
container, and close the container.
Observation of medication pass in the main building on 9/3/08 at 8:55 AM
5
15.
revealed a med tech standing at the medication cart placing the following
medications for resident #8 into a medicine cup: Norvasc (high blood
pressure) 5 mg, Seroquel (schizophrenia, bipolar disorder) 400 mg, Lopressor
(high blood pressure) 50 mg, Depakote (seizures, bipolar disorder) 500 mg,
Haldol (schizophrenia) 5 mg, Tegretol (seizures, bipolar disorder) 20 mg, and
Klonopin (seizures, panic disorder) 1 mg. The medications were placed in a
medication cup at the cart and the cup of medications was given to the
resident. The med tech did not, in the presence of the resident, read the label,
open the container, remove the prescribed amount of medication from the
container, and close the container.
Observation of medication pass in the main building on 9/3/08 at 8:55 AM
revealed a med tech standing at the medication cart placing the following
medications for resident #9 in a medication cup: Glipizide (antidiabetic agent)
5 mg, Vesicare (overactive bladder) 5 mg, Actophusmet 15-500, Lopid (high
cholesterol) 600 mg, Haldol (schizophrenia) 5 mg, Iron 325 mg, Seroquel
(schizophrenia, bipolar disorder) 300 mg, Phenobarbital (sedative, seizures)
64.8, and Depakote (seizures, bipolar disorder) 500 mg. The medications were
placed in a cup at the cart and handed to the resident who was next to the cart.
The med tech did not, in the presence of the resident, read the label, open the
container, remove the prescribed amount of medication from the container,
and close the container.
. On 9/4/08 at 3:10 PM the administrator, assistant administrator, and director
of nursing were made aware of the observations.
That the failure to provide assistance with self administration, and having unlicensed staff
administer medications to 4 of 4 residents (#1, 2, 8, 9) during the medication pass observation, is
in violation of law.
16.
That the Agency determined that this deficient practice presented an imminent danger to
the residents and serious physical or emotional harm would result and cited Respondent for a
State Class I deficiency.
17.
The regulatory provisions of the Fla. Admin. Code (2007) that are pertinent to this
alleged violation read as follows:
429,.256(3)(a) and (b) Assistance with self-administration of medication
(a) Taking the medication, in its previously dispensed, properly labeled container, from
where it is stored, and bringing it to the resident.
(b) In the presence of the resident, reading the label, opening the container, removing a
prescribed amount of medication from the container, and closing the container.
6
OK
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$5,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to 58A-
5.0185 (3)(c) Fla. Admin. Code (2007).
COUNT III
Respondent failed to have a licensed nurse administer medications to 4 of 4 residents (#1, 2,
8, 9) during medication pass observation. Medication pass observation was observed on all
units (2 of 2) and 2 medication technicians (med techs) were observed; and facility failed to
administer psychiatric medications in accordance with the physician order for 1 resident,
#12, who had to be admitted to a crisis stabilization unit for care.
18. The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
19. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
20. That based on observations, staff interview, and record review the facility failed to have a
licensed nurse administer medications to 4 of 4 residents (#1, 2, 8, 9) during medication pass
observation. Medication pass observation was observed on all units (2 of 2) and 2 medication
technicians (med techs) were observed; and facility failed to administer psychiatric medications
in accordance with the physician order for 1 resident, #12, who had to be admitted to a crisis
stabilization unit for care, the same being in violation of law. The findings include:
a. Observation of medication pass on the special care unit on 9/3/08 at 8:40 AM
revealed a med tech standing at the medication cart (alone) placing
medications in a cup for resident #2: Roxanol (narcotic analgesic) 5 mg,
Glipizide (antidiabetic agent) 5 mg , Lasix (diuretic) 20 mg, Zoloft
(antidepressant) 100 mg, K+ 10 meq (potassium), Risperdal (antipsychotic
agent) 0.5 mg, Trilisate (arthritis) 500 mg, Tylenol (analgesic) 500 mg,
Valium (anxiety disorders) 2 mg. The medications were placed in a
7
medication cup and crushed except Roxanol was added to 8 ounces of orange
juice (OJ). The medications were taken to the resident at the breakfast table in
the common dining room. :
. The med tech did not, take the medication, in its dispensed, properly labeled
container, from where it was stored and bring it to the resident. The med tech
did not, in the presence of the resident, read the label, open the container,
remove the prescribed amount of medication from the container, and close the
container.
. The med tech poured the crushed medications on the top of the resident’s
pancakes and placed the OJ with the Roxanol at the residents place. The med
tech stated she has to feed the resident and this is the only way they can get
the resident to take the medication. The med tech was busy with other things
and left the resident sitting at the dining room table with the crushed
medications on top of the pancakes and the OJ with the Roxanol on the table.
There were two other residents sitting at the dining room table with resident
#2 at this time. Both residents were confused and wandered. These three
residents were not supervised or observed by the medication tech. Resident #2
ate half of the food and drank half of the OJ. Resident #2 did not receive
Natural Tears one gtt (drop) in both eyes as ordered. The med tech stated the
medication was not available from the pharmacy.
. Observation of medication pass on the special care unit on 9/3/08 at 8:15 AM
revealed a med tech aide standing at the medication cart alone placing the
following medications for resident #1 in a medication cup: Cogentin
(antiparkinson's disease) one 20 milligrams (mg) and one Mestinon
(myasthenia gravis) 60 mg. The medications were placed in a medication cup
at the cart then taken in the cup to the resident. The medication was poured
on to the bed and the resident picked the medication up and took the
medication. The med tech did not, take the medication, in its dispensed,
properly labeled container, from where it was stored and bring it to the
resident. The med tech did not, in the presence of the resident, read the label,
open the container, remove the prescribed amount of medication from the
container, and close the container.
Observation of medication pass in the main building on 9/3/08 at 8:55 AM
revealed a med tech standing at the medication cart placing the following
medications for resident #8 into a medicine cup: Norvasc (high blood
pressure) 5 mg, Seroquel (schizophrenia, bipolar disorder) 400 mg, Lopressor
(high blood pressure) 50 mg, Depakote (seizures, bipolar disorder) 500 mg,
Haldol (schizophrenia) 5 mg, Tegretol (seizures, bipolar disorder) 20 mg, and
Klonopin (seizures, panic disorder) 1 mg. The medications were placed in a
medication cup at the cart and the cup of medications was given to the
resident. The med tech did not, in the presence of the resident, read the label,
open the container, remove the prescribed amount of medication from the
container, and close the container.
21.
Observation of medication pass in the main building on 9/3/08 at 8:55 AM
revealed a med tech standing at the medication cart placing the following
medications for resident #9 in a medication cup: Glipizide (antidiabetic agent)
5 mg, Vesicare (overactive bladder) 5 mg, Actophusmet 15-500, Lopid (high
cholesterol) 600 mg, Haldol (schizophrenia) 5 mg, Iron 325 mg, Seroquel
(schizophrenia, bipolar disorder) 300 mg, Phenobarbital (sedative, seizures)
64.8, and Depakote (seizures, bipolar disorder) 500 mg. The medications were
placed in a cup at the cart and handed to the resident who was next to the cart.
The med tech did not, in the presence of the resident, read the label, open the
container, remove the prescribed amount of medication from the container,
and close the container.
. On 9/4/08 at 3:10 PM the administrator, assistant administrator, and director
of nursing were made aware of the observations. Record review of “chart
notes “revealed resident #12 was admitted 8/29/08 at-1:00 p.m.
. Record review of the Department of Elder Affairs/Assisted Living Facility
Form 1823 health assessment for resident #12 dated 8/27/08 indicated a
diagnosis of schizoaffective disorder bipolar type, organic affective disorder
with confusion and psychosis. Medications ordered on the health assessment
included: Risperdal (schizophrenia, bipolar disorder) 3 milligrams twice daily,
Cogentin (antiparkinson's disease) 1 milligram (mg) two times a day as
needed, Haldol (schizophrenia) 5 milligrams every 6 hours as needed, Ativan
(anxiety) 2 milligrams every 6 hours as needed, Klonopin (seizures, panic
disorder) 0.5 milligrams two times day, and Klonopin 0.5 milligrams, 2, at HS
(bedtime). In addition, Haldol and Ativan had lines drawn through them and
the notation “D/C‘d 8/29/08 “.
Review of the MOR indicated: Risperdal 3 mg on 8/30/08 at 8:00 a.m. not
given as evidenced by initials circled for that time and day. Risperdal 3 mg
given only once on 9/1/08 with no time documented. Should have been given
twice daily. Cogentin 1 mg on 8/30/08 at 8:00 a.m. not given as evidenced by
initials circled for that time and day. Haldol 5 mg given 9/1/08 at 8:00 a.m.
and 9/2/08 at 9/2/08 with no documented reason or response. This was after
the discontinuation date of 8/29/08. Ativan “four Ativan to equal 2 mg” given
9/1/08 at 1:00 p.m. “c/o anxiety “with no response documented. This was
after the discontinuation date of 8/29/08. Ranitidine 50 mg. was given 9/1/08
once with no time documented. There was no physician order for this
medication. The Klonopin was not administered as it was not on the MOR to
be given.
On 9/2/08 at 10:00 a.m. the resident exhibited erratic behavior, saw sparks
coming out of the light sockets, room was in disarray, wandered in/out of
other residents ' rooms and went through their belongings. Resident had to be
admitted to a crisis stabilization unit for care and treatment.
The failure to have a licensed nurse administer medications to 4 of 4 residents (#1, 2, 8,
9
9) during medication pass; and the failure to administer psychiatric medications in accordance
with the physician order for 1 resident, #12, who had to be admitted to a crisis stabilization unit
for care, reflects the Respondent’s failure to provide physician prescribed medications the same
being in violation of law.
22. That the Agency determined that this deficient practice presented an imminent danger to
the residents and serious physical or emotional harm would result and cited Respondent for a
State Class I deficiency |
23. The regulatory provisions of the Fla. Admin. Code and Florida Statues (2007) that is
pertinent to this alleged violation read as follows:
58A-5.0185 (4)(a) Medication Practices.
MEDICATION ADMINISTRATION.
(a) For facilities which provide medication administration a staff member, who is
licensed to administer medications, must be available to administer medications in
accordance with a health care provider’s order or prescription label.”
* OOK
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$5,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to §
58A 5.0185 (4)(a) Florida Admin. Code.
COUNT IV
The Respondent failed to maintain an accurate medication observation record (MOR) for 1
(#12) of 22 sampled residents, who had to be admitted to a crisis stabilization unit for care
and services.
24, The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
25. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
26. That based on record review and staff interview the facility failed to maintain an accurate
medication observation record (MOR) for 1 (#12) of 22 sampled residents, who had to be
admitted to a crisis stabilization unit for care and services, the same being in violation of law.
The findings include:
a. Record review of “chart notes" revealed resident was admitted 8/29/08 at
1:00 p.m. Record review of the Department of Elder Affairs/Assisted Living
Facility Form 1823 health assessment for resident #12 dated 8/27/08 indicated
a diagnosis of schizoaffective disorder bipolar type, organic affective disorder
with confusion and psychosis. Medications ordered on the health assessment
included: Risperdal (schizophrenia, bipolar disorder) 3 milligrams twice daily,
Cogentin (antiparkinson's disease) 1 milligram (mg) two times a day as
needed, Haldol (schizophrenia) 5 milligrams every 6 hours as needed, Ativan
(anxiety) 2 milligrams every 6 hours as needed, Klonopin (seizures, panic
disorder) 0.5 milligrams two times day, and Klonopin 0.5 milligrams, 2, at HS
(bedtime). In addition, Haldol and Ativan had lines drawn through them and
the notation “D/C‘d 8/29/08 “.
b. Review of the MOR indicated: Risperdal 3 mg on 8/30/08 at 8:00 a.m. not
given as evidenced by initials circled for that time and day. Risperdal 3 mg
given only once on 9/1/08 with no time documented. Should have been given
twice daily. Cogentin 1 mg on 8/30/08 at 8:00 a.m. not given as evidenced by
initials circled for that time and day. Haldol 5 mg given 9/1/08 at 8:00 a.m.
and 9/2/08 at 9/2/08 with no documented reason or response. This was after
the discontinuation date of 8/29/08. Ativan “four Ativan to equal 2 mg” given
9/1/08 at 1:00 p.m. “c/o anxiety “with no response documented. This was
after the discontinuation date of 8/29/08. Ranitidine 50 mg. was given 9/1/08
once with no time documented. There was no physician order for this
medication. The Klonopin was not administered as it was not on the MOR to
be given.
c. On 9/2/08 at 10:00 a.m. the resident exhibited erratic behavior, saw sparks
coming out of the light sockets, room was in disarray, wandered in/out of
other residents ' rooms and went through their belongings. Resident had to be
admitted to a crisis stabilization unit for care and treatment.
27. The failure to maintain an accurate medication observation record (MOR) for 1 (#12) of
22 sampled residents, who had to be admitted to a crisis stabilization.unit for care and services,
reflects the Respondent’s failure to maintain an accurate daily medication observation record, the
same being in violation of law.
28. That the Agency determined that this deficient practice presented an imminent danger to
the residents and serious physical or emotional harm would result and cited Respondent for a
i
State Class I deficiency.
29. The regulatory provisions of the Fla. Admin. Code and Florida Statues (2007) that is
pertinent to this alleged violation read as follows:
58A-5.0185 (5)(c) Medication Practices.
MEDICATION RECORDS. The facility shall maintain a daily medication observation
record (MOR) for each resident who receives assistance with self-administration of
medications or medication administration. A MOR must include the name of the resident and
any known allergies the resident may have; the name of the resident’s health care provider,
the health care provider’s telephone number; the name, strength, and directions for use of
each medication; and a chart for recording each time the medication is taken, any missed
dosages, refusals to take medication as prescribed, or medication errors. The MOR must be
immediately updated each time the medication is offered or administered.
OOF
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$5,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to §
58A-5.0185 (5)(c) Florida Admin. Code.
COUNTY
Respondent failed to store medications in a locked cart out of reach of wandering and
confused residents on the specialty unit, which has the potential for harm.
The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth herein.
30. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
31. Based on observation the facility failed to store medications in a locked cart out of reach
of wandering and confused residents on the specialty unit which has the potential for harm, the
same being in violation of law. The findings include:
a. Observation of medication pass on the special care unit on 9/3/08 at 8:40 AM
revealed a med tech standing at the medication cart (alone) placing
medications in a cup for resident #2: Roxanol (narcotic analgesic) 5 mg,
Glipizide (antidiabetic agent) 5 mg , Lasix (diuretic) 20 mg, Zoloft
(antidepressant) 100 mg, K+ 10 meq (potassium), Risperdal (antipsychotic
12
agent) 0.5 mg, Trilisate (arthritis) 500 mg, Tylenol (analgesic) 500 mg,
Valium (anxiety disorders) 2 mg. The medications were placed in a
medication cup and crushed except Roxanol was added to 8 ounces of orange
juice (OJ). The medications were taken to the resident at the breakfast table in
the common dining room. The med tech did not, in the presence of the
resident, read the label, open the container, remove the prescribed amount of
medication from the container, and close the container.
b. The med tech poured the crushed medications on the top of the resident’s
pancakes and placed the OJ with the Roxanol at the residents place, The med
tech stated she has to feed the resident and this is the only way they can get
the resident to take the medication. The med tech was busy with other things
and left the resident sitting at the dining room table with the crushed
medications on top of the pancakes and the OJ with the Roxanol on the table.
There were two other residents sitting at the dining room table with resident
#2 at this time. Both residents were confused and wandered. These three
residents were not supervised or observed by the medication tech. Resident #2
ate half of the food and drank half of the OJ. Resident #2 did not receive
Natural Tears one gtt (drop) in both eyes. The med tech stated the medication
was not available from the pharmacy.
c. Observation on 9/3/08 at 8:15 AM on the specialty care unit the following
medications were noted on top of an unattended medication cart, out of view
of the med tech: Namenda (dementia) 10 mg and Lisinopril (high blood
pressure) 5 mg and Aricept (dementia) 10 mg. The med tech went out the
back door on two occasions leaving the medications on top of the cart with
confused/wandering residents present.
32. That the failure to store medications in a locked cart out of reach of wandering and
confused residents on the specialty unit which has the potential for harm, the same being in
violation of law.
33. That the Agency determined that this deficient practice was related to the personal care of
the resident that directly threatened the health, safety, or security of the resident and cited
Respondent for a State Class II deficiency.
34. The regulatory provisions of the Fla. Admin. Code (2007) that is pertinent to this alleged
violation read as follows:
58A-5.0185 (6)(b) Medication Practices.
MEDICATION STORAGE AND DISPOSAL. Centrally stored medications must be:
1. Kept in a locked cabinet, locked cart, or other locked storage receptacle, room, or area
13
at all times;
2. Located in an area free of dampness and abnormal temperature, except that a
medication requiring refrigeration shall be refrigerated. Refrigerated medications shall be
secured by being kept in a locked container within the refrigerator, by keeping the
refrigerator locked, or by keeping the area in which refrigerator is located locked;
3. Accessible to staff responsible for filling pill-organizers, assisting with
self-administration, or administering medication. Such staff must have ready access to
keys to the medication storage areas at all times; and
4. Kept separately from the medications of other residents and properly closed or sealed.
* OK OK
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$1,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to §
58A-5.0185 (6)(b), Florida Admin. Code.
COUNT VI
Respondent failed to ensure that prescriptions for 14 (#1, 2, 3, 4, 5, 7, 10, 11,12, 13, 14, 15,
16, 17) of 22 residents were filled in a timely, manner which jeopardized the health of
residents #3, #4 and #12.
35. The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
36. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
37. That based on resident record review, family interviews, and an interview with staff and
the owner, the facility failed to ensure that prescriptions for 14 (#1, 2, 3, 4, 5, 7, 10, 11, 12, 13,
14, 15, 16, 17) of 22 residents were filled in a timely manner, which jeopardized the health of
residents #3, #4 and #12, the same being in violation of law. The findings include:
a. Review of resident #3 's Department of Elder Affairs/Assisted Living Facility
(DOEA/ALF) Form 1823 health assessment (no date) indicated a diagnosis of
chest pain and shortness of breath and assistance with activities of daily
living. A second health assessment dated 1/12/07 indicated diagnoses of
chronic obstructive pulmonary disease, smoker, coronary artery disease with
atrial fibulation, anxiety, agitation, dementia. This assessment included a
14
mo
physician order for Nitroglycerin (angina pectoris) 0.3 milligrams (mg.) patch
on at 0600 and off at 2200. Hospice progress notes dated 8/28/08 indicate
diagnosis of debility.
Review of medication observation record (MOR) indicated the following:
May 2008 indicated the resident to receive Nitro-Dur 0.3 mg every morning
and remove every evening. The following dates indicate initials that are
circled: May 1, May 2, May 3, May 4, May 5, May 6, and 7/08. Interview
with staff on 9/3/08 at 10:00 AM stated we circle our initials when the
resident refuses or the medication was not given and document why on the
back of the MOR. Review of the back of the May 2008 MOR revealed staff
notation for 5/1-7/08 stating Nitro-patch on order. Another MOR dated May
2008 indicated Nitro-patch ON at 8:00 a.m. was circled (not given) May 8, 9,
12, 13, 14, 15, 16, 17, 18, 19, 22, 23, 24, 25 and on the back of the MOR it
was documented for 5/5, 5/8, 5/9, 5/10 on order/not available.
June 2008 indicated Nitro-patch circled on June 26, 27, 28, 29, 30 and on the
back documented not available for 6/26, 6/27, 6/28, 6/29, 6/30.
Protonix (erosive esophagitis associated with gastro-esophageal reflux
disorder) was circled as not given on June 27, 28, 29, blank on 30 and.31; and
on the back documented on order 6/28/08, 6/29/08, and 6/31/08.
July 2008 indicated Nitro-patch was circled as not given July 1, 2, 3, 4, 5, 6,
and on the back documented not available July 1,2,3,5,6,7,8,9,10, and 11.
August 2008 indicated Nitro-patch not available for the following dates:
August 12 and 14. Lexapro (major depressive disorder) 10 mg was not
available on 8/5/08. Amaryl (diabetes) 1 mg was not available August 2 and 3.
Ultram (analgesic) 50 mg not available August 2-3.
Review of Hospice progress notes from 8/13/08-8/25/08 indicate resident had
wheezing and rhonchi, no pain, good appetite; gets up and out to smoke and
eat meals, denies pain, edema in feet/ankles continues up to 2+ at times,
rhonchi; dated 8/25/08 indicated resident continues to have irregular pulse
with lower extremity pitting edema 2 + at feet with 1+ at mid shins. Has
respiratory wheezing and rhonchi, refuses respiratory treatment or oxygen.
Resident becomes short of breath with ambulation of 40 feet. Mental status
prevents resident from comprehending results of non-compliance with
treatment orders.
Interview with administrator 9/4/08 2:10 PM stated the resident went to the
emergency room on 8/30/08. She stated she was on call for the facility and
received a call stating the resident was short of breath, B/P 160/110 and face
very red.
Review of the record including the chart notes lacked documentation that the
missed medications listed above were called to the family and or physician.
The record also lacked documentation about the resident becoming ill 8/30/08
and being admitted to the hospital.
The resident was still in the hospital as of 9/5/08.
Review of resident #4 's DOEA/ALF Form 1823 health assessment dated
1/10/08 indicated a diagnosis of schizoaffective disorder depressive type.
Record review of MORs indicated the following: May 2008 an order for
Vistaril (anxiety) 25 mg for anxiety as needed ordered 1/08. Vistaril was
given for anxiety 18 times in the month of May 2008. June 2008 the resident
15S
received Vistaril 15 times. Review of the MOR's prior to May 2008 revealed
the resident did not require that many doses of anti-anxiety medications.
. Review of the chart notes dated 7/13/08 indicated the resident cut her wrist
with a razor, sprayed self with hairspray and threatened to set self on fire.
Resident was transported to hospital and was admitted to a psychiatric unit.
The resident returned to the assisted living facility on 7/17/08.
. August 2008 MOR indicated Effexor (major depressive disorder, general
anxiety disorder, social anxiety) was not available/on order August 1-21 and
August 24-26.
. The September 2008 MOR indicated Effexor not given 9/1/08, not available.
. Other medications that were not available as indicated on the MOR's include:
Lescol for high cholesterol not given 8/1-11/08 with notation written on MOR
stating authorization required. Protonix (erosive esophagitis associated with
gastro-esophageal reflux disorder) 40 mg one a day was not given 8/5-31/08,
9/1 and 2/08 with notation on back of MOR stating prior authorization
needed. On 9/1/08 notation written on MOR stating order change. Reglan
(gastro-esophageal reflux disorder) 5 mg three times a day was not given 2
times 9/1/08.
. August 2008 MOR indicated a new order for Cephalexin (antibiotic) 500 mg
two times a day for 10 days starting 8/19/08. The MOR indicated the
medication was given for 10 days ending on the 29" which would be 20 pills.
Review of the label indicated the same information and those 20 pills
dispensed. Count in the container indicated 10 pills remaining even though
staff signed as given. Resident only received half of ordered antibiotics.
September 2008 MOR indicated to give Cephalexin 500 mg two times a day
for 5 days. As of 9/4/08 there were no initials documented on MOR.
Interview with staff on 9/4/08 at 2:35 PM indicated this order should not be
here the antibiotic was given and completed in August 2008 and could not
explain why 10 pills were remaining.
Lotrimin cream was ordered to be applied daily for 15 days ending 9/8/08.
The medication was not given September 1, 2, 3, 4, 2008. ;
Record review of the DOEA/ALF Form 1823 health assessment for resident
#12 dated 8/27/08 indicated a diagnosis of schizoaffective disorder bipolar
type, organic affective disorder with confusion and psychosis. Medications
ordered on the health assessment included: Risperdal (schizophrenia, bipolar
disorder) 3 milligrams twice daily, Cogentin (antiparkinson's disease) 1
milligram (mg) two times a day as needed, Haldol (schizophrenia) 5
milligrams every 6 hours as needed, Ativan (anxiety) 2 milligrams every 6
hours as needed, Klonopin (seizures, panic disorder) 0.5 milligrams two times
day, and Klonopin 0.5 milligrams, 2, at HS (bedtime).
. In addition, Haldol and Ativan had lines drawn through them and the notation
» “DIC*d 8/29/08 “.
. Review of the MOR indicated: Risperdal 3 mg on 8/30/08 at 8:00 a.m. not
given as evidenced by initials circled for that time and day. Risperdal 3 mg
given only once on 9/1/08 with no time documented. Should have been given
twice daily. Cogentin 1 mg on 8/30/08 at 8:00 a.m. not given as evidenced by
initials circled for that time and day. Haldol 5 mg given 9/1/08 at 8:00 a.m.
and 9/2/08 at 9/2/08 with no documented reason or response. This was after
16
the discontinuation date of 8/29/08. Ativan “four Ativan to equal 2 mg” given
9/1/08 at 1:00 p.m. "c/o anxiety " with no response documented. This was
after the discontinuation date of 8/29/08. Ranitidine 50 mg. was given 9/1/08
once with no time documented. There was no physician order for this
medication. The Klonopin was not administered as it was not on the MOR to
be given.
w. On 9/2/08 at 10:00 a.m. the resident exhibited erratic behavior, saw sparks
coming out of the light sockets, room was in disarray, wandered in/out of
other residents ' rooms and went through their belongings. Resident had to be
admitted to a crisis stabilization unit for care and treatment.
x. Record review for resident #1 indicated a diagnosis of myasthenia gravis and
paranoid schizophrenia. Review of the MOR dated August 2008 indicated
Mestinon (myasthenia gravis) 60 mg one every 8 hours for Myasthenia Gravis
was refused August 2,3,4,5,6,7,9,10,11,12,13,14,22,,29,30 and on order for
8/30. Review of MOR for dates 9/1, 2 & 3 notes medication refused.
y. August 2008 MOR revealed Mestinon and Cogentin were not available and
“on order “August 30 and August 31, 2008.
z. The record lacked documentation that family and or physician was called
concerning the refusal of medication for documented diagnosis of myasthenia
gravis.
aa. Record review for resident #2 indicated a diagnosis of schizophrenia,
dementia, Alzheimer's disease, diabetes, and Hospice for Failure to Thrive.
bb. The May 2008 MOR’s indicated Morphine (narcotic analgesic) 0.25 mg two
times a day on order/not available May 5-11. The following medications were
not available/on order: Senna (stool softener) 2 tabs at HS (bedtime) on May
1-13, Valium (anxiety) 2 mg one every 12 hours and Trilasate (arthritis) 500
mg one, two times day on May 17 and 18.
cc. September 2008 MOR indicated Refresh eye gtts (drops) daily on order/not
available September 1-2. The MOR dated 5/08 indicated to give Reminyl 12
mg two times a day. No signatures noted as given and the back lacked
comments on why. This was repeated on MOR’s for 8/08 and 9/08. Written
on MOR by drug indicates prior authorization requested. The record lacked
documentation that the pharmacy or physician was called to clarified. Staff
found an order to discontinue the medication on 5/12/08 but the MOR never
reflected this. ,
dd. Review of MOR’s for 5/08, 8/08 & 9/08 indicated the resident refused
medications 57 times.
ee. The record lacked documentation that the family and or physician were
notified of the refusal of medications.
ff. DOEA/ALF Form 1823 health assessment dated 5/11/07 revealed resident #5
had diagnoses of altered mental status, senile dementia, anxiety, depression,
agitation, diabetes, and osteoporosis.
gg. Review of July 2008 MOR indicated the following medications were not
available/on order from the pharmacy: Viactiv Calctum Chew one three times
a day was not available in facility from 7/14/08 through 7/31/08. Benadryl 25
mg one every 6 hours was not given from 7/26-31/08. Synthroid
(hypothyroidism) 75 mcg one daily was not given from 7/29-31/08. Actonel
(osteoporosis) 35 mg one daily was not given 7/7/08 and “on order
17
“documented. There was no documentation the medication was given the
entire month of July 2008.
hh. Review of August 2008 MOR indicated the following medications were not
available/on order from pharmacy: Viactiv Calcium Chew was not given from
8/1-15/08. Actonel (osteoporosis) 35 mg one daily was not given the entire
month of August 2008 and documented “not available “. Remeron
(depression) 45 mg one daily was not given August 1-2 " on order “August 8
through August 14 “on order” August 15-22 circled as not given (19" is
blank) August 26 circled as not given. Risperdal (schizophrenia, bipolar
disorder) 2 mg daily was circled as not given August 1 resident refused and
August 17, 19, 22, 26-31 were all blank.
ii. Record review of chart notes dated 6/22/08 indicated resident has rash with
severe itching, possible scabies. On 6/26/08 notes indicate the resident was
treated for scabies, see Drs orders.
Further record review lacked documentation that family and or physician were
notified medications were not being administered as ordered by the physician.
Interview with staff on 9/4/08 at 2:10 PM had no comment about why family
and physician were not called.
kk. DOEA/ALF Form 1823 health assessment dated 5/30/08 for resident #7
indicated diagnoses of diabetes, hypertension, and peripheral vascular disease.
Il. Record review July 2008 MOR indicated the following medications were not
given/on order from pharmacy: Neurontin (seizures, neuropathic pain) 100 mg
one three times a day was not given 7/1-8/08. Order was changed to
Neurontin 300 mg one three times a day starting 7/10/08. This medication
was not given 7/10-14/08. Lactinex (promote normal bacterial flora in the
intestinal tract) one three times a day was not given 7/1-30/08 and noted to be
“not available “or “med on order “. Clonidine (high blood pressure) 0.1 mg.
every 12 hours was ordered on August 18, 2008. The medication was circled
as not given until the first dose at 8:00 p.m. on 8/20/08. The medication was
circled as not given August 30-31, 2008. Blood pressure was to be taken twice
daily when this medication was given. Blood pressure was only taken once a
day from August 18-27, 2008 and only once daily September 1, 3, 4, and not
taken at all on September 2, 2008. Blood pressure ranges from 168/108 to
124/76,
mm. Review of the chart notes lacked documentation that family or physician
was notified of medications not given.
nn. DOEA/ALF Form 1823 with no date and incomplete revealed for resident #10
diagnoses of hypertension, arthritis, obesity, history of breast cancer and
hypothyroidism. Also noted “medication administration “.
oo. Record review of July 2008 MOR indicated the following medications were
refused by resident: Vitamin one daily, Verapamil (angina pectoris, high
blood pressure) 240 mg, Tylenol (analgesic) 325 mg two, two times a day,
Clonidine (high blood pressure) 0.2 mg one two times a day, Combivent AER
2 puffs every 12 hours, Synthroid (hypothyroidism) 25 mcg one time a day,
Mavik (high blood pressure) 4 mg one, one time a day, ASA 325 mg, Calcarb
600 mg, Nolvadex (breast cancer), Persantine (antiplatelet agent, vasodilator),
Iron, Indapamide (high blood pressure), Micro-K (potassium), Medications
were refused by resident 17 times. ;
Ji-
18
Pp.
qq.
Ss.
tt.
uu.
The record lacked documentation the family or physician were called.
Review of the MOR dated September 2008 indicated Combivent AER inhaler
was not given September 1,2,3,4, 2008. The back of the MOR stated “meds
on order “, The record lacked documentation the family or physician were
called.
. DOEA/ALF Form 1823 dated 5/30/07 for resident #11 indicated diagnoses of
chronic schizophrenia and dementia, hypertension and diabetic:
Record review of August 2008 MOR indicated the following medications not
given/on order from pharmacy: Risperdal (schizophrenia, bipolar disorder) 4
mg two times a day was refused 40 times. Seroquel (schizophrenia, bipolar
disorder) 200 mg one time a day was refused 18 times. Namenda (dementia)
10 mg one time a day was refused 19 times. Cogentin (anti-Parkinson’s) 1 mg
one time a day was refused 17 times. Verapamil (angina pectoris, high blood
pressure) 120 ER one two times a day was refused 12 times and not signed as
given 17 times. ASA 81 mg one time a day was refused 4 times. Vitamin one
time a day was refused 7 times. Coreg (heart failure) 3.125 mg was refused 23
times. Triamcinolon cream 0.025 % two times a day was refused 34 times.
Haldol (schizophrenia) 5 mg one every 4 hours was not given/on order from
pharmacy August 1,2,3,4,5, 2008 then the resident refused the medication
from 8/7-31/08.
Review of September 2008 MOR indicated Risperdal 4 mg was not given and
“on order “September 2, 3, 8, 2008. Further review of the record indicated the
physician was notified 2/21/08 that the resident was refusing medications. On
5/31/08 a note indicated the resident was in the hospital and was intubated.
The resident began Dialysis 6/08 and returned from hospital. The facility
notified the physician the resident refuses to go to Dialysis, no mention the
resident is refusing medications since 2/21/08.
DOEA/ALF Form 1823 not dated and incomplete for resident #13 indicated a
diagnosis of paranoid schizophrenia.
. Record review of August 2008 MOR indicated Miralax 17 Grams one
package daily was " not available “ August 22, 23, 24, 2008, Topamax
(seizures) 25 mg two tablets two times a day was not given and documented
as "not available" or "on order" August 22-27, 2008, Seroquel
(schizophrenia, bipolar disorder) 200 mg two at bedtime and Seroquel 100 mg
one at bedtime were not given and documented as "on order" August 23-26,
2008. Record review of September 2008 MOR indicated Bethanechol
(urinary retention) 10 mg one two times a day was not given and " on order
“September 1, 2008, Topamax (seizures) 25 mg two times a day was not
given and " on order “September 1, 2008 and Haldol (schizophrenia) 10 mg
two at bedtime and Haldol 5 mg one at bedtime was not given and " on order
“September 1, 2008. Review of the record lacked documentation the family or
physician was notified.
ww. Record review of MOR for resident # 17 indicated Zocor (high
XX,
cholesterol) 20 mg half a tab at bedtime was not given and “on order “August
17-31, 2008. Further review of the record lacked evidence the family or
physician was notified.
Record review of MOR for resident #14 indicated Prilosec (ulcer, heartburn,
gastroesophageal reflux disease) 20 mg one daily was not given and
19
documented as "on order" August 1, 2, 3, 4, 2008. Captopril (high blood
pressure, heart failure) 25 mg one half tab two times a day was not given and
documented as “on order “August 15-30, 2008. Flomax (benign prostatic
hyperplasia) 0.4 mg one daily was not given and documented as “on order
“August 29, 2008. Further record review lacked documentation the family
or physician was notified.
yy. Review of resident #15 MOR dated 8/08 indicated Miralax 17 gram one
packet daily was not given and documented "on order" August 23- 24, 2008
and September 1, 2, 3, 2008. Ativan 2 milligrams, 1 tablet per day as needed
for anxiety was given twice on August 4, 6, 8, 2008. Further record review
lacked documentation the family or physician was notified.
zz. Review of MOR for resident #16 indicated Advair Disk one puff two times a
day was not given and documented “on order “August 7-29, 2008. Kenalog
0.1% cream was not available from August 11-26, 2008. Further record
review lacked documentation that family or physician was notified.
aaa. Interview with director of nursing, assistant administrator and
administrator 9/4/08 5:00 PM regarding medication errors and omissions
revealed staff stated we know we have problems--- we've only been here since
July 2008.
38. That the failure to ensure that prescriptions for 14 (#1, 2, 3, 4, 5, 7, 10, 11,12, 13, 14, 15,
16, 17) of 22 residents were filled in a timely manner, which jeopardized the health of residents
#3, #4 and #12, the same being in violation of law.
39. That the Agency determined that this deficient practice presented an imminent danger to
the residents and serious physical or emotional harm would result and cited Respondent for a
State Class I deficiency.
40. The regulatory provisions of the Fla. Admin. Code (2007) that is pertinent to this alleged
violation read as follows: .
58A-5.0185 (7)(f) Medication Practices.
MEDICATION LABELING AND ORDERS. The facility shall make every reasonable
effort to ensure that prescriptions for residents who receive assistance with self-
administration of medication or medication administration are filled or refilled in a timely
manner,
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$5,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to §
20
58A-5.0185 (7)(f) Florida Admin. Code.
COUNT VII
Respondent failed to provide assistance with self administration of medication and had
unlicensed staff administer medications (A610); facility failed to have a licensed nurse
administer medications and facility failed to administer psychiatric medications in
accordance with the physician order (A613); failed to maintain an accurate medication
observation record (A615); facility failed to store medications in a locked cart out of reach
of wandering and confused residents (A619); facility failed to ensure that prescriptions
were filled in a timely manner (A631); facility failed to notify family, physician, responsible
party of resident changes in conditions of residents (A706); facility failed to serve diets as
ordered by the physician, failed to follow the menu, and failed to have therapeutic meals
listed on menus(A806).
41. The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
42. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
43. Based on observation, interview and record review facility failed to provide necessary
care and services to resident as evidenced by facility failed to provide assistance with self
administration of medication and had unlicensed staff administer medications (A610); facility
failed to have a licensed nurse administer medications and facility failed to administer
psychiatric medications in accordance with the physician order (A613); failed to maintain an
accurate medication observation record (A615); facility failed to store medications in a locked
cart out of reach of wandering and confused residents (A619); facility failed to ensure that
prescriptions were filled in a timely manner (A631); facility failed to notify family, physician,
21
responsible party of resident changes in conditions of residents (A706); facility failed to serve
diets as ordered by the physician, failed to follow the menu, and failed to have therapeutic meals
listed on menus(A806), the same being in violation of law.
44, That the failure to provide necessary care and services to resident as evidenced by facility
failed to provide assistance with self administration of medication and had unlicensed staff
administer medications (A610); facility failed to have a licensed nurse administer medications
and facility failed to administer psychiatric medications in accordance with the physician order
(A613); failed to maintain an accurate medication observation record (A615); facility failed to
store medications in a locked cart out of reach of wandering and confused residents (A619);
facility failed to ensure that prescriptions were filled in a timely manner (A631); facility failed to
notify family, physician, responsible party of resident changes in conditions of residents (A706);
facility failed to serve diets as ordered by the physician, failed to follow the menu, and failed to
have therapeutic meals listed on menus(A806).
45. That the Agency determined that this deficient practice presented an imminent danger to
the residents and serious physical or emotional harm would result and cited Respondent for a
State Class I deficiency.
46. The regulatory provisions of the Fla. Admin. Code (2007) that is pertinent to this alleged
violation read as follows:
58A-5.0182 Resident Care Standards.
An assisted living facility shall provide care and services appropriate to the needs of
residents accepted for admission to the facility.
(1) SUPERVISION. Facilities shall offer personal supervision, as appropriate for each
resident, including the following:
(a) Monitor the quantity and quality of resident diets in accordance with Rule 58A-5.020,
(by Daly observation by designated staff of the activities of the resident while on the
premises, and awareness of the general health, safety, and physical and emotional
well-being of the individual.
(c) General awareness of the resident’s whereabouts. The resident may travel
22
independently in the community.
(d) Contacting the resident’s health care provider and other appropriate party such as the
resident’s family, guardian, health care surrogate, or case manager if the resident exhibits
a significant change; contacting the resident’s family, guardian, health care surrogate, or
case manager if the resident is discharged or moves out.
(e) A written record, updated as needed, of any significant changes as defined in 58A-
5.0131(33), F.A.C., any illnesses which resulted in medical attention, major incidents,
changes in the method of medication administration, or other changes which resulted in
the provision of additional services.
(2) SOCIAL AND LEISURE ACTIVITIES. Residents shall be encouraged to participate
in social, recreational, educational and other activities within the facility and the
community.
(a) The facility shall provide an ongoing activities program. The program shall provide
diversified individual and group activities in keeping with each resident’s needs, abilities,
and interests.
(b) The facility shall consult with the residents in selecting, planning, and scheduling
activities, The facility shall demonstrate residents’ participation through one or more of
the following methods: resident meetings, committees, a resident council, suggestion box,
group discussions, questionnaires, or any other form of communication appropriate to the
size of the facility.
(c) Scheduled activities shall be available at least six (6) days a week for a total of not
less than twelve (12) hours per week. Watching television shall not be considered an
activity for the purpose of meeting the twelve (12) hours per week of scheduled activities
unless the television program is a special one-time event of special interest to residents of
the facility. A facility whose residents choose to attend day programs conducted at adult
day care centers, senior centers, mental health centers, or other day programs may count
those attendance hours towards the required twelve (12) hours per week of scheduled
activities. An activities calendar shall be posted in common areas where residents
normally congregate.
(d) If residents assist in planning a special activity such as an outing, seasonal festivity, or
an excursion, up to three (3) hours may be counted toward the required activity time.
(3) ARRANGEMENT FOR HEALTH CARE. In order to facilitate resident access to
needed health care, the facility shall, as needed by each resident:
(a) Assist residents in making appointments and remind residents about scheduled
appointments for medical, dental, nursing, or mental health services.
(b) Provide transportation to needed medical, dental, nursing or mental health services, or
arrange for transportation through family and friends, volunteers, taxi cabs, public buses,
and agencies providing transportation for persons with disabilities.
(c) The facility may not require residents to see a particular health care provider.
(4) ACTIVITIES OF DAILY LIVING. Facilities shall offer supervision of or assistance
with activities of daily living as needed by each resident. Residents shall be encouraged
to be as independent as possible in performing ADLs.
(5) NURSING SERVICES.
(a) Pursuant to Section 429.255, F.S., the facility may employ or contract with a nurse to:
1. Take or supervise the taking of vital signs;
2. Manage pill-organizers and administer medications as described under Rule 58A
5.0185, F.AC.;
3. Give prepackaged enemas pursuant to a physician’s order; and ~
23
4. Maintain nursing progress notes.
(b) Pursuant to Section 464.022, F.S., the nursing services listed in paragraph (a) may
also be delivered in the facility by family members or friends of the resident provided the
family member or friend does not receive compensation for such services.
(6) RESIDENT RIGHTS AND FACILITY PROCEDURES.
(a) A copy of the Resident Bill of Rights as described in Section 429.28, F.S., or a
summary provided by the Long-Term Care Ombudsman Council shall be posted in full
view in a freely accessible resident area, and included in the admission package provided
pursuant to Rule 58A-5.0181, F.A.C.
(b) In accordance with Section 429.28, F.S., the facility shall have a written grievance
procedure for receiving and responding to resident complaints, and for residents to
recommend changes to facility policies and procedures. The facility must be able to
demonstrate that such procedure is implemented upon receipt of a complaint.
(c) The address and telephone number for lodging complaints against a facility or facility
staff shall be posted in full view in a common area accessible to all residents. The
addresses and telephone numbers are: the District Long-Term Care Ombudsman Council,
1(888)831-0404; the Advocacy Center for Persons with Disabilities, 1(800)342-0823; the
Florida Local Advocacy Council, 1(800)342-0825; and the Agency Consumer Hotline
1(888)419-3456,
(d) The statewide toll free telephone number of the Florida Abuse Hotline “1(800)96-
ABUSE or 1(800)962-2873” shall be posted in full view in a common area accessible to
all residents. .
(e) The facility shall have a written statement of its house rules and procedures which
shall be included in the admission package provided pursuant to Rule 58A-5.0181,
F.A.C. The rules and procedures shall address the facility’s policies with respect to such
issues, for example, as resident responsibilities, the facility’s alcohol and tobacco policy,
medication storage, the delivery of services to residents by third party providers, resident
elopement, and other administrative and housekeeping practices, schedules, and
requirements.
(f) Residents may not be required to perform any work in the facility without
compensation, except that facility rules or the facility contract may include a requirement
that residents be responsible for cleaning their own sleeping areas or apartments. If a
resident is employed by the facility, the resident shall be compensated, at a minimum, at
an hourly wage consistent with the federal minimum wage law.
(g) The facility shall provide residents with convenient access to a telephone to facilitate
the resident’s right to unrestricted and private communication, pursuant to Section
429.28(1)(d), F.S. The facility shall not prohibit unidentified telephone calls to residents.
For facilities with a licensed capacity of 17 or more residents in which residents do not
have private telephones, there shall be, at a minimum, an accessible telephone on each
floor of each building where residents reside.
(h) Pursuant to Section 429.41, F.S., the use of physical restraints shall be limited to half
bed rails, and only upon the written order of the resident’s physician, who shall review
the order biannually, and the consent of the resident or the resident’s representative. Any
device, including half-bed rails, which the resident chooses to use and can remove or
avoid without assistance shall not be considered a physical restraint.
(7) THIRD PARTY SERVICES. Nothing in this rule chapter is intended to prohibit a
resident or the resident’s representative from independently arranging, contracting, and
paying for services provided by a third party of the resident’s choice, including a licensed
24
home health agency or private nurse, or receiving services through an out-patient clinic,
provided the resident meets the criteria for continued residency and the resident complies
with the facility’s policy relating to the delivery of services in the facility by third parties.
The facility’s policies may require the third party to coordinate with the facility regarding
the resident’s condition and the services being provided. Pursuant to subsection (6), the
facility shall provide the resident with the facility’s policy regarding the provision of
services to residents by non-facility staff.
(8) ELOPEMENT STANDARDS.
(a) Residents Assessed at Risk for Elopement. All residents assessed at risk for elopement
or with any history of elopement shall be identified so staff can be alerted to their needs
for support and supervision.
1. As part of its resident elopement response policies and procedures, the facility shall
make, at a minimum, a daily effort to determine that at risk residents have identification
on their persons that includes their name and the facility’s name, address, and telephone
number. Staff attention shall be directed towards residents assessed at high risk for
elopement, with special attention given to those with Alzheimer’s disease and related
disorders assessed at high risk.
2. Ata minimum, the facility shall have a photo identification of at risk residents on file
that is accessible to all facility staff and law enforcement as necessary. The photo
identification shall be made available for the file within 10 calendar days of admission. In
the event a resident is assessed at risk for elopement subsequent to admission, photo
identification shall be made available for the file within 10 calendar days after a
determination is made that the resident is at risk for elopement. The photo identification
may be taken by the facility or provided by the resident or resident’s family/caregiver.
(b) Facility Resident Elopement Response Policies and Procedures. The facility shall
develop detailed written policies and procedures for responding to a resident elopement.
At a minimum, the policies and procedures shall include:
1. An immediate staff search of the facility and premises;
2. The identification of staff responsible for implementing each part of the elopement
response policies and procedures, including specific duties and responsibilities;
3. The identification of staff responsible for contacting law enforcement, the resident’s
family, guardian, health care surrogate, and case manager if the resident is not located
pursuant to subparagraph (8)(b)1.; and
4. The continued care of all residents within the facility in the event of an elopement.
(c) Facility Resident Elopement Drills. The facility shall conduct resident elopement
drills pursuant to Sections 429.41(1)(a)3. and 429.41(1)(), F.S.
(9) OTHER STANDARDS. Additional care standards for residents residing in a facility
holding a limited mental health, extended congregate care or limited nursing services
license are provided in Rules 58A-5.029, 58A-5.030 and 58A-5.031, F.A.C., respectively.
* KOK
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$5,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to §
58A- 5.0182 Fla. Admin. Code (2007).
25
COUNT VIII
Respondent failed to notify family, physician, or responsible party of resident changes in
condition for 3 of 22 residents #3, #4, #12.
47. The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
48. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
49. Based on record review, complainant and staff interview it was determined the facility
failed to notify family, physician, responsible party of resident changes in condition for 3 of 22
residents #3, #4, #12, the same being in violation of law. The findings include:
a.
Review of resident #3 's Department of Elder Affairs/Assisted Living Facility
(DOEA/ALF) Form 1823 health assessment (no date) indicated a diagnosis of
chest pain and shortness of breath and assistance with activities of daily
living. A second health assessment dated 1/12/07 indicated diagnoses of
chronic obstructive pulmonary disease, smoker, coronary artery disease with
atrial fibulation, anxiety, agitation, dementia. This assessment included a
physician order for Nitroglycerin (angina pectoris) 0.3 milligrams (mg.) patch
on at 0600 and off at 2200. Hospice progress notes dated 8/28/08 indicate
diagnosis of debility.
Review of medication observation record (MOR) indicated the following:
May 2008 indicated the resident to receive Nitro-Dur 0.3 mg every morning
and remove every evening. The following dates indicate initials that are
circled: May 2, May 2, May 3, May 4, May 5, May 6, and 7/08. Interview
with staff on 9/3/08 at 10:00 AM stated we circle our initials when the
resident refuses or the medication was not given and document why on the
back of the MOR. Review of the back of the May 2008 MOR revealed staff
notation for 5/1-7/08 stating Nitro-patch on order. Another MOR dated May
2008 indicated Nitro-patch ON at 8:00 a.m. was circled (not given) May 8, 9,
12, 13, 14, 15, 16, 17, 18, 19, 22, 23, 24, 25 and on the back of the MOR it
was documented for 5/5, 5/8, 5/9, 5/10 on order/not available.
June 2008 indicated Nitro-patch circled on June 26, 27, 28, 29, 30 and on the
back documented not available for 6/26, 6/27, 6/28, 6/29, 6/30. Protonix
(erosive esophagitis associated with gastro-esophageal reflux disorder) was
circled as not given on June 27, 28, 29, blank on 30 and 31; and on the back
documented on order 6/28/08, 6/29/08, and 6/31/08.
July 2008 indicated Nitro-patch was circled as not given July 1, 2, 3, 4, 5, 6,
and on the back documented not available July 1,2,3,5,6,7,8,9,10, and 11.
August 2008 indicated Nitro-patch not available for the following dates:
26
fg
August 12 and 14. Lexapro (major depressive disorder) 10 mg was not
available on 8/5/08. Amaryl (diabetes) 1 mg was not available August 2 and 3.
Ultram (analgesic) 50 mg not available August 2-3.
Review of Hospice progress notes from 8/13/08-8/25/08 indicate resident had
wheezing and rhonchi, no pain, good appetite; gets up and out to smoke and
eat meals, denies pain, edema in feet/ankles continues up to 2+ at times,
thonchi; dated 8/25/08 indicated resident continues to have irregular pulse
with lower extremity pitting edema 2 + at feet with 1+ at mid shins. Has
respiratory wheezing and rhonchi, refuses respiratory treatment or oxygen.
Resident becomes short of breath with ambulation of 40 feet. Mental status
prevents resident from comprehending results of non-compliance with
treatment orders.
Interview with administrator 9/4/08 2:10 PM stated the resident went to the
emergency room on 8/30/08. She stated she was on call for the facility and
received a call stating the resident was short of breath, B/P 160/110 and face
very red.
Review of the record including the chart notes lacked documentation that the
missed medications listed above were called to the family and or physician.
The record also lacked documentation about the resident becoming ill 8/30/08
and being admitted to the hospital. The resident was still in the hospital as of
9/5/08.
Review of resident #4 's DOEA/ALF Form 1823 health assessment dated
1/10/08 indicated a diagnosis of schizoaffective disorder depressive type.
Record review of MORs indicated the following:
May 2008 an order for Vistaril (anxiety) 25 mg for anxiety as needed ordered
1/08. Vistaril was given for anxiety 18 times in the month of May 2008. June
2008 the resident received Vistaril 15 times. Review of the MOR's prior to
May 2008 revealed the resident did not require that many doses of anti-
anxiety medications.
Review of the chart notes dated 7/13/08 indicated the resident cut her wrist
with a razor, sprayed self with hairspray and threatened to set self on fire.
Resident was transported to hospital and was admitted to a psychiatric unit.
The resident returned to the assisted living facility on 7/17/08.
August 2008 MOR indicated Effexor (major depressive disorder, general
anxiety disorder, social anxiety) was not available/on order August 1-21 and
August 24-26.
. The September 2008 MOR indicated Effexor not given 9/1/08, not available.
Other medications that were not available as indicated on the MOR's include:
Lescol for high cholesterol not given 8/1-11/08 with notation written on MOR
stating authorization required. Protonix (erosive esophagitis associated with
gastro-esophageal reflux disorder) 40 mg one a day was not given 8/5-31/08,
9/1 and 2/08 with notation on back of MOR stating prior authorization
needed. On 9/1/08 notation written on MOR stating order change. Reglan
(gastro-esophageal reflux disorder) 5 mg three times a day was not given 2
times 9/1/08.
August 2008 MOR indicated a new order for Cephalexin (antibiotic) 500 mg
two times a day for 10 days starting 8/19/08. The MOR indicated the
medication was given for 10 days ending on the 29" which would be 20 pills.
27
50.
<
Review of the label indicated the same information and those 20 pills
dispensed. Count in the container indicated 10 pills remaining even though
staff signed as given. Resident only received half of ordered antibiotics.
September 2008 MOR indicated to give Cephalexin 500 mg two times a day
for 5 days. As of 9/4/08 there were no initials documented on MOR.
Interview with staff on 9/4/08 at 2:35 PM indicated this order should not be
here the antibiotic was given and completed in August 2008 and could not
explain why 10 pills were remaining.
Lotrimin cream was ordered to be applied daily for 15 days ending 9/8/08.
The medication was not given September 1, 2, 3, 4, 2008.
Review of facility records revealed no evidence facility staff notified the
resident's physician or responsible party of the change of condition or the
missed medication doses.
Record review of “chart notes " revealed resident was admitted 8/29/08 at
1:00 p.m. Record review of the DOEA/ALF Form 1823 health assessment for
resident #12 dated 8/27/08 indicated a diagnosis of schizoaffective disorder
bipolar type, organic affective disorder with confusion and psychosis.
Medications ordered on the health assessment included: Risperdal
(schizophrenia, bipolar disorder) 3 milligrams twice daily, Cogentin
(antiparkinson's disease) 1 milligram (mg) two times a day as needed, Haldol
(schizophrenia) 5 milligrams every 6 hours as needed, Ativan (anxiety) 2
milligrams every 6 hours as needed, Klonopin (seizures, panic disorder) 0.5
milligrams two times day, and Klonopin 0.5 milligrams, 2, at HS (bedtime).
In addition, Haldol and Ativan had lines drawn through them and the notation
“DiC‘d 8/29/08 “.
Review of the MOR indicated: Risperdal 3 mg on 8/30/08 at 8:00 a.m. not
given as evidenced by initials circled for that time and day. Risperdal 3 mg
given only once on 9/1/08 with no time documented. Should have been given
twice daily. Cogentin 1 mg on 8/30/08 at 8:00 a.m. not given as evidenced by
initials circled for that time and day. Haldol 5 mg given 9/1/08 at 8:00 a.m.
and 9/2/08 at 9/2/08 with no documented reason or response. This was after
the discontinuation date of 8/29/08. Ativan “four Ativan to equal 2 mg” given
9/1/08 at 1:00 p.m. "c/o anxiety " with no response documented, This was
after the discontinuation date of 8/29/08. Ranitidine 50 mg. was given 9/1/08
once with no time documented. There was no physician order for this
medication.
The Klonopin was not administered as it was not on the MOR to be given.
. On 9/2/08 at 10:00 a.m. the resident exhibited erratic behavior, saw sparks
coming out of the light sockets, room was in disarray, wandered in/out of
other residents ' rooms and went through their belongings. Resident had to be
admitted to a crisis stabilization unit for care and treatment.
Review of facility records revealed no evidence facility staff notified the
resident's physician or responsible party of the change of condition or the
missed medication doses.
That the failure to notify family, physician, or responsible party of resident changes in
condition for 3 of 22 residents #3, #4, #12, the same being in violation of law.
28
51. That the Agency determined that this deficient practice presented an imminent danger to
the residents and serious physical or emotional harm would result and cited Respondent for a
State Class I deficiency.
52. The regulatory provisions of the Fla. Admin. Code (2007) that is pertinent to this alleged
violation read as follows:
58A-5.0182 (1)(d) Resident Care Standards.
SUPERVISION. Contacting the resident’s health care provider and other appropriate
party such as the resident’s family, guardian, health care surrogate, or case manager if the
resident exhibits a significant change; contacting the resident’s family, guardian, health
care surrogate, or case manager if the resident is discharged or moves out.
* OK
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$5,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to §
58A-5.0182 (1)(d) Florida Admin. Code.
COUNT IX
Respondent failed to follow the menu and failed to serve therapeutic diets as ordered by the
physician for 8 (#3, 9, 10, 16, 18, 19, 21, 22) of 22 sampled resident.
53. The Agency re-alleges and incorporates paragraphs (1) through (5) as if fully set forth
herein.
54. That on September 4, 2008, the Agency conducted an assisted living facility complaint
survey of the Respondent facility.
55. Based on observation and record review it was determined the facility failed to follow the
menu and failed to serve therapeutic diets as ordered by the physician for 8 (#3, 9, 10, 16, 18, 19,
21, 22) of 22 sampled resident, the same being in violation of law. The findings include:
a. Review of the current menu indicated only regular diets are served with no
concentrated sweets and no added salt. Interview with administrator, assistant
administrator, and director of nursing on 9/4/08 at 1:40 PM stated we don't
29
serve any diets other that regular.
b. Record review of the health assessment (HA) for resident #3 indicated a
diagnoses of chest pain and shortness of breath with an order for Low
Fat/Low Cholesterol diet.
c. Record review of the HA for resident #9 indicated a diagnosis of diabetes
mellitus (DM) with an order for a diabetic diet.
d. Record review of the HA for resident #16 indicated a diagnosis of DM with an
order for diabetic dict. ,
¢. Record review of the HA for resident #18 indicated a diagnosis of (DM) with
a diet order for 1800 calorie diet.
f. Record review of the HA for resident #19 indicated a diagnosis of DM with an
order for diabetic diet.
g. Record review of the HA for resident #21 indicated a diagnosis of DM with an
order for 1800 calorie diet.
h. Record review of the HA for resident #22 indicated a diagnosis of DM with an
order for 1800 calorie diet.
i. There was no evidence the facility had menus for Low Fat/Low Cholesterol,
Diabetic or 1800 Calorie diets and there was no evidence the residents with
these diet orders received a therapeutic diet in accordance with these
restrictions.
j. Observation 9/3/08 and 9/4/09 at 8:00 AM on the special care unit revealed
resident #10 asking for coffee during breakfast. Interview with administrator,
assistant administrator, and director of nursing at the same time stated that
coffee is on the menu, however, they can't have coffee on the special care unit
because coffee is hot and residents might burn themselves.
56. The failure to follow the menu and failed to serve therapeutic diets as ordered by the
physician for 8 (#3, 9, 10, 16, 18, 19, 21, 22) of 22 sampled residents, the same being in violation
of law.
57. That the Agency determined that this deficient practice was related to the personal care of
the resident that directly threatened the health, safety, or security of the resident and cited
Respondent for a State Class II deficiency.
58. The regulatory provisions of the Fla. Admin. Code (2007) that is pertinent to this alleged
violation read as follows:
58A-5.020 (1)(c) Food Service Standards.
GENERAL RESPONSIBILITIES. When food service is provided by the facility, the
administrator or a person designated in writing by the administrator shall: provide regular
meals which meet the nutritional needs of residents, and therapeutic diets as ordered by
the resident’s health care provider for resident’s who require special diets.
30
WHEREFORE, the Agency intends to impose an administrative fine in the amount of
$1,000.00 against Respondent, an assisted living facility in the State of Florida, pursuant to §
58A-5.020 (1)(c) Florida Admin. Code.
COUNT X
59. The Agency re-alleges and incorporates paragraphs one (1) through five (5) and the
remainder of this Complaint as if fully recited herein.
60. That the Agency may revoke any license issued under Part I of Chapter 429 Florida
Statutes (2007) for the citation of three (3) or more cited Class I deficiencies, three (3) or more
cited Class II deficiencies that have been cited on a single survey and have not been corrected
within the specified time period. Section 429.14(1) (e) Florida Statutes (2007).
61. That the Respondent has been cited five (5) widespread State Class I deficiencies (Counts
I, II, Ill, VI, VID, two (2) isolated State Class I deficiencies, and one widespread State Class II
deficiency on an Agency complaint visit on September 4, 2008.
62. That the Agency may revoke any license issued under Section 408.815(1) (d), Florida
Statutes (2007) for a demonstrated pattern of deficient performance.
63. That based thereon, the Agency seeks the revocation of the Respondent’s licensure as its
primary relief.
64. That should the Respondent admit the facts herein by action or inaction, the Petitioner
shall enter an Order revoking the Respondent’s.
WHEREFORE, the Agency intends to revoke the license of the Respondent to operate an
assisted living facility in the State of Florida, pursuant to §§ 408.815(1) (d) and 429.14(1) (e),
31
Florida Statutes (2007).
CLAIM FOR RELIEF
WHEREFORE, the State of Florida, Agency for Health Care Administration, respectfully
requests that this court:
(A) Make factual and legal findings in favor of the Agency on Count I through Count IX;
(B) Recommend an administrative fine against Respondent in the amount of $37,000 for
Count I, I, II, IV, V, VI, VII, VII, [X, as well as a survey fee of $500.00, pursuant
to Sections 400.419(10), Florida Statutes (2007).
(C) Revoke Respondent’s Assisted Living Facility License number 7258;
(D) Assess attorney’s fees and costs; and
(E) Grant all other general and equitable relief allowed by law.
Respectfully submitted this day of September 2008
Bart O. Moore, Esquire
Fla. Bar. No. 0768715
Counsel for Petitioner
u Agency for Health Care Administration
S 2727 Mahan Drive, MS #3
Pel “shassec, Florida 32308
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Docket for Case No: 08-005413
Issue Date |
Proceedings |
Apr. 16, 2010 |
Motion to Re-Open File filed. (DOAH CASE NO. 10-2182 ESTABLISHED)
|
Mar. 30, 2010 |
Response to Motion to Re-Open File filed.
|
Mar. 25, 2010 |
Notice of Appearance (filed by S.Haston).
|
Feb. 09, 2009 |
Order Closing File. CASE CLOSED.
|
Feb. 02, 2009 |
Agreed Motion to Continue Final Hearing filed.
|
Jan. 21, 2009 |
Notice of Hearing (hearing set for February 12, 2009; 10:00 a.m., Central Time; Pensacola, FL).
|
Dec. 04, 2008 |
Notice of Appearance and Substitution of Counsel (filed by M. David) filed.
|
Nov. 05, 2008 |
Joint Response to Initial Order filed.
|
Oct. 29, 2008 |
Initial Order.
|
Oct. 28, 2008 |
Administrative Complaint filed.
|
Oct. 28, 2008 |
Petition for Formal Administrative Proceeding filed.
|
Oct. 28, 2008 |
Motion to Dismiss Petition for Formal Administrative Proceeding filed.
|
Oct. 28, 2008 |
Amended Petition for Formal Administrative Proceeding filed.
|
Oct. 28, 2008 |
Order on Motion to Dismiss Petition for Formal Administrative Proceedings filed.
|
Oct. 28, 2008 |
Notice (of Agency referral) filed.
|