F 0641
Ensure each resident receives an accurate assessment.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record review and interview, the facility failed to ensure resident assessments accurately reflected the
residents' status for 1 of 3 residents reviewed, Resident #105.
Residents Affected - Few
Findings include:
Review of Resident #105's physician order dated 12/22/2023 read, OK to D/C [discharge] to home on
[DATE].
Review of Resident #105's Discharge Summary showed the summary read, 6. Reason for
discharge/discharge diagnosis: resident and family request.
Review of Resident #105's discharge return not anticipated Minimum Data Set (MDS) dated [DATE]
showed the resident was discharged to short-term general hospital.
During an interview on 3/19/2024 at 12:16 PM, Staff I, Licensed Practical Nurse (LPN), stated, The
discharge status for the patient was entered incorrectly. The patient was not discharged to a hospital. The
patient was discharged home.
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 12
Event ID:
105308
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0655
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Create and put into place a plan for meeting the resident's most immediate needs within 48 hours of being
admitted
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record review and interview, the facility failed to develop and implement a baseline care plan to provide
effective and person-centered care within 48 hours for 2 of 2 residents with tracheostomy, Residents #256
and #257.
Findings include:
Review of Resident #256's admission record showed the resident was admitted on [DATE] with the
diagnoses that included acute respiratory failure with hypercapnia, pneumonia, unspecified organism,
unspecified protein calorie malnutrition, generalized muscle weakness, tracheostomy status, gastrostomy
status, chronic kidney disease, cerebrovascular disease, generalized anxiety disorder, adult failure to thrive,
and essential primary hypertension.
Review of Resident #256's medical record revealed no care plan or care planned interventions related to
tracheostomy.
Review of Resident #257's admission record showed the resident was admitted on [DATE] with diagnoses
that included cerebral infarction (stroke), acute respiratory failure with hypoxia (low oxygen levels in body
tissues), chronic systolic (congestive) heart failure, Alzheimer's disease, tracheostomy status (a surgical
opening in the neck for a tube to provide an airway and remove secretions from the lungs), and seizures.
Review of Resident #257's medical record revealed no care plan or care planned interventions related to
tracheostomy, oxygen, and suctioning needs.
During an interview on 3/19/2024 at 8:22 AM, the Director of Nursing stated, I do not see a baseline care
plan with interventions related to the trach [tracheostomy].
During an interview on 3/20/2024 at 9:45 AM, Staff I, Licensed Practical Nurse (LPN), stated, There is no
baseline care plan in PCC [point click care] for the tracheostomy. I usually document it on paper and do a
comprehensive within 21 days. I did not have this completed. We should do a baseline and it would be
important for the care for the trachs.
Review of the facility policy and procedures titled Baseline Care Plan with the last approval date of
12/29/2023 read, Procedure: The facility will develop and implement a baseline care plan for each resident
that includes the instructions needed to provide effective and person-centered care of the resident that
meet the professional standards of quality care. The baseline care plan will: 1. Be developed within 48
hours of a resident's admission.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 2 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
Provide appropriate treatment and care according to orders, resident’s preferences and goals.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record review and interview, the facility failed to ensure residents who required long-acting insulin received
insulin per physician orders for 2 of 6 residents reviewed for unnecessary medications, Residents #17 and
#60.
Residents Affected - Few
Findings include:
1. Review of Resident #17's admission record showed the resident was admitted on [DATE] with the
diagnoses that included metabolic encephalopathy, diabetes mellitus due to underlying condition with
hyperosmolarity without nonketotic hyperglycemic hyperosmolar coma (a serious complication of diabetes
mellitus with high blood sugar levels and dehydration), unspecified atrial fibrillation (an irregular heartbeat),
acute kidney failure, peripheral vascular disease, hyperlipidemia, and chronic venous hypertension.
Review of Resident #17's physician order dated 1/10/2024 read, Order Summary: Insulin Glargine
Subcutaneous Solution Pen-injector 100 unit/ml [milliliter] (Insulin Glargine) Inject 12 unit subcutaneously at
bedtime for DM [diabetes mellitus] Order Summary: May check glucose PRN [as needed] if exhibiting sx
[symptoms] of Hypo [low] or Hyper [high] Glycemia [blood sugar] as needed for sx of Hypo or Hyper
glycemia Call MD [Medical Doctor] if BS [blood sugar] is < 60 or > 500.
Review of Resident #17's Medication Administration Record (MAR) for February 2024 for administration of
Insulin Glargine revealed the MAR was coded as 13 (glucose out of parameters) on 2/12/2024 at 9:00 PM,
and coded as 10 (vitals out of parameters) on 2/20/2024, 2/28/2024, and 2/29/2024 at 9:00 PM.
Review of Resident #17's progress notes dated 2/28/2024 at 10:03 PM showed a medication administration
note reading, Held due to glucose 49.
Review of Resident # 17's progress notes from 2/12/2024 through 2/29/2024 revealed no physician
notification of insulin being held and blood sugar of 49, no recheck of blood sugar on 2/28/2024 after blood
sugar of 49, no assessment for signs and symptoms of hypoglycemia and no treatment for blood sugar of
49.
Review of Resident #17's MAR for March 2024 for administration of Insulin Glargine revealed the MAR was
coded as 13 on 3/5/2024 and 3/11/2024 at 9:00 PM, and coded as 10 on 3/12/2024 and 3/15/2024 at 9:00
PM.
Review of Resident #17's progress notes from 3/1/2024 through 3/17/2024 revealed no physician
notification of insulin being held.
During an interview on 3/19/2023 at 10:51 AM, the Director of Nursing (DON) verified that the insulin was
documented as held and stated, Long-acting insulin should not be held and does not have any parameters
to hold it. When her [Resident #17's] blood sugar was 49, I do not see any repeat blood sugars
documented. There should be a recheck of blood sugar when below 60. We do have orders for
hypoglycemia in place and should have called the doctor. I don't see any notes documenting he [the doctor]
was notified.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 3 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
Level of Harm - Minimal harm
or potential for actual harm
During a telephone interview on 3/19/2024 at 10:57 AM, Staff F, Registered Nurse (RN), stated, I did hold
these insulins on [Resident #17's name]. She is a brittle diabetic and I remember at least once that it was
like 49 and I held it. It [the insulin] does not have any parameters to hold it, but I still held it. That's a nursing
judgement call. I did not call or let the doctor know. I should have called when her blood sugar was below
60.
Residents Affected - Few
During a telephone interview on 3/19/2024 at 11:33 AM, Staff B, Licensed Practical Nurse (LPN), stated, If I
held the medication it was because her blood sugar was out of range. It was too low to give. We do have
parameters to hold insulin, so that's what I did. Long-acting insulin should be held when the blood sugars
are below 150 like the orders say. I should have a note if I called the doctor.
2. Review of Resident #60's admission record showed the resident was admitted on [DATE] with diagnoses
that included type 2 diabetes mellitus with unspecified complications, acquired absence of right leg below
knee, acute kidney failure, and essential primary hypertension.
Review of Resident #60's physician order dated 12/1/2023 read, Insulin Aspart Solution, Inject as per
sliding scale.
Review of Resident #60's physician order dated 2/1/2024 read, Lantus Solution 100 unit/ml (Insulin
Glargine), Inject 20 units subcutaneously one time a day related to type 2 diabetes mellitus with unspecified
complications.
Review of Resident #60's MAR for February 2024 for administration of Insulin Aspart revealed no
documentation on 2/7/2024, 2/8/2024 and 2/11/2024 at 10:00 PM. Further review of the MAR for
administration of Lantus Solution revealed no documentation on 2/7/2024 and on 2/11/2024 at 9:00 PM.
Review of Resident #60's MAR for March 2024 for administration of Lantus Solution revealed the MAR was
coded as 2 (drug refused) on 3/1/2024 and 3/7/2024 at 6:00 AM, and coded as 9 (other/see notes) on
3/6/2024.
Review of Resident #60's nursing progress note dated 3/1/2024 read, Patient refused Lantus 20 units
stating she didn't want to take it because she is concerned it will drop her blood sugar to low. This writer
explained to patient how long acting insulin worked. Patient stated she understood but still did not want to
take it at this time.
Review of Resident #60's progress notes from 3/1/2024 through 3/17/2024 revealed no physician
notification of insulin being held.
During an interview on 3/19/2024 at 10:53 AM, the DON verified that insulin was held and documented as
held and there were blanks on the MAR for Resident #60 and stated, There seems to be no documentation
for when or if the insulin was given and there are some drug refusals. I expect the nurses to document that
they notified the doctor or on call when this happens.
During a telephone interview on 3/19/2024 at 11:52 AM, the Medical Doctor (MD) stated, The staff should
notify us when they are holding insulin. Long-acting insulin typically doesn't have orders to hold, but we may
need to discuss this as an option to get that done in the future. I would expect nurses to use some type of
judgement to hold when the blood sugars are below 60 and a patient is symptomatic. I do expect orders to
be followed. I don't think as I review that there was any true harm or potential for any adverse
consequences in having held these medications. I should be notified if
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 4 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
patients are refusing their insulin, so I can speak with them and educate them about the risks of refusing
and make a treatment plan they will stick to. I do want staff to notify us when they are holding medications.
During an interview on 3/20/2024 at 6:08 AM, Staff G, LPN, stated, I did hold her [Resident #60's] insulin.
She refused it. I should have called the doctor, but no I did not. She does sometimes refuse her long-acting
insulin when she thinks her blood sugar is too low.
Review of the facility policy and procedure titled Diabetes Management with an approval date of 12/29/2023
read, Policy: It will be the policy of this facility to provide appropriate care to residents with diabetes mellitus.
Nursing measures and physician orders will be implemented to minimize the risk of hypo/hyperglycemia.
Procedure: 1. Residents diagnosed with diabetes mellitus (or other condition requiring blood glucose
monitoring and control) will receive insulin, oral hypoglycemic medications and/or an individually prescribed
diet according to physician order . 5. Staff will provide glucose monitoring, medication administration,
laboratory testing and diet per physician orders . 7. Staff should report signs and symptoms of
hypoglycemia to the physician. Many residents receiving insulin and oral hypoglycemic have parameters as
to when the physician should be notified . 10. Nursing interventions, per physician orders, may vary for
residents experiencing hypoglycemia depending on the severity and symptoms of the resident as residents'
behavior is different depending on their sensitivity to hypoglycemia. Responsive residents that are able to
swallow may receive juice or other rapidly absorbed glucose as an intervention. Responsive residents that
are unable to swallow or unresponsive residents may receive oral glucose paste to buccal mucosa,
intramuscular glucagon, or IV 50% dextrose and notify the physician for further orders . 13. Report non
compliance with physician orders to the physician and/or resident representative, if applicable. 14.
Document pertinent information regarding medication administration, changes in condition, education or
interventions in clinical record.
Review of the facility policy and procedure titled 6.0 General Dose Preparation and Medication
Administration with the last revision date of 1/1/2022 and the last approval date of 12/29/2023 read,
Applicability: The Policy 6.0 sets forth the procedures relating to general dose preparation and medication
administration. Facility staff should also refer to Facility policy regarding medication administration and
should comply with Applicable Law and the State Operations Manual when administering medications.
Procedure . 6. After medication administration, Facility staff should take all measures required by Facility
policy and Applicable Law, including, but not limited to the following: 6.1 Document necessary medication
administration/treatment information (e.g., when medications are opened, when medications are given,
injection site of a medication, if medications are refused, PRN medications, application site) on appropriate
forms.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 5 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0689
Level of Harm - Minimal harm
or potential for actual harm
Ensure that a nursing home area is free from accident hazards and provides adequate supervision to
prevent accidents.
Based on observation, interview, and record review, the facility failed to ensure resident rooms were free of
accident hazards for 1 of 3 residents reviewed for accidents, Resident #76.
Residents Affected - Few
Findings include:
During an observation on 3/17/2024 at 9:37 AM, there was an open can of green beans at Resident #76's
bedside with a sharp metal edge exposed. Approximately 3/4 of the sharp lid was bent backwards and
approximately 1/4 of the lid remained intact.
During an interview on 3/17/2024 at 9:38 AM, Resident #76 stated she had opened the can with her can
opener the night before. When asked if she had ever cut or injured herself on the open can or with the can
opener, Resident #76 stated, I have not yet.
During an interview on 3/17/2024 at 9:45 AM, the Director of Nursing (DON) confirmed that the can of
green beans had exposed metal edge and should not have been there and could be a danger.
Review of Resident #76's physician order dated 11/21/2023 read, Eliquis Oral Tablet 5 MG [milligram]
(Apixaban), Give 5 mg by mouth two times a day for a fib.
Review of Resident #76's care plan initiated on 8/24/2023 read, Focus: [Resident #76's name] is at risk for
abnormal bleeding, hemorrhage, and bruising related to anticoagulant use for atrial fibrillation.
During an interview on 3/18/2024 at 1:15 PM, the Social Services Director (SSD) stated she did not
personally buy canned foods for Resident #76; however, the grandson of Resident #76 brings in food for her
all the time. When asked if she was aware that Resident #76 had a personal can opener in her room that
she used to open cans of food, the SSD stated she was unaware of this, and residents should not have can
openers in their room as the can opener could pose a risk of getting cut or injured.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 6 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure residents received respiratory care
consistent with professional standards of practice for 1 of 3 residents reviewed for respiratory care,
Resident #257.
Residents Affected - Few
Findings include:
Review of Resident #257's admission record showed the resident was admitted on [DATE] with diagnoses
that included cerebral infarction (stroke), acute respiratory failure with hypoxia (low oxygen levels in body
tissues), chronic systolic (congestive) heart failure, Alzheimer's disease, tracheostomy status (a surgical
opening in the neck for a tube to provide an airway and remove secretions from the lungs), and seizures.
Review of Resident #257's physician order dated 3/15/2024 read, Trach- Encourage and assist resident
with us of humidified oxygen 28%/5 liters via trach collar every shift.
During an observation on 3/17/2024 at 3:17 PM, Resident #257 had a tracheostomy collar mask with no
humidification, and the oxygen concentrator was set on 4 liters per minute.
Review of Resident #257's physician order dated 3/18/2024 read, Trach- Encourage and assist resident
with us of humidified oxygen 28% via trach collar every shift.
During an observation on 3/18/2024 at 1:28 PM, Resident #257 had a tracheostomy mask collar, and the
oxygen concentrator was set on 3 liters per minute.
During an observation on 3/19/2024 at 7:41 AM, Resident #257 had a tracheostomy mask collar and the
oxygen concentrator was running at 3 liters per minute.
During an interview on 3/19/2024 at 8:11 AM, Staff C, Licensed Practical Nurse (LPN), confirmed that
oxygen was running at 3 liters and stated, I honestly have not seen an oxygen order for 28%. It's usually set
at liters, not a percent. I don't know how many liters of oxygen make 28% by the trach collar.
During an interview on 3/19/2024 at 8:22 AM, the Director of Nursing (DON) stated, The oxygen should run
at whatever the order calls for. I don't know if the staff know what liters per minute make 28% oxygen. The
concentrator should not be at 3, 4 or 5 liters. The oxygen should be set at 2 liters per minute. I expect staff
to follow doctor's orders for oxygen.
Review of the facility policy and procedure titled Tracheostomy Care and Suctioning/Oxygen with the last
approval date of 12/29/2023, read, Policy: The facility will ensure that residents who need respiratory care,
including tracheostomy care and tracheal suctioning, is provided care consistent with professional
standards of practice, the comprehensive person-centered care plan and resident goals and preferences.
Procedures . 2. The facility will provide necessary respiratory care and services, such as oxygen therapy as
ordered by the physician, treatments, mechanical ventilation, tracheostomy care and/or suctioning.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 7 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure medications were labeled and stored
in accordance with currently accepted professional principles in 4 of 4 medication carts reviewed for
medication storage.
Findings include:
During an observation on [DATE] at 8:35 AM, Medication Cart #1 was unlocked and unattended. There
were two residents walking by the medication cart. Staff B, Licensed Practical Nurse (LPN), returned to the
medication cart at 8:38 AM. The medication cart was unattended and unlocked for three minutes.
During an interview on [DATE] at 8:38 AM, after coming back to the medication cart, Staff B, LPN, stated, I
shouldn't have done that, but I wasn't really gone that long.
During an observation of Medication Cart #1 on [DATE] at 8:38 AM with Staff B, LPN, there were two
opened Novolog insulins with no date opened or expiration date, one opened Lantus insulin with no date
opened or expiration date, and one opened bottle of artificial tears with no date opened or expiration date.
During an interview on [DATE] at 8:39 AM, Staff B, LPN, stated, All insulin should have the date opened
and expiration dates. I don't know when eye drops expire.
During an observation of Medication Cart #2 on [DATE] at 8:40 AM with Staff C, LPN, there were one
opened Lispro insulin pen with no date opened or expiration date, one opened bottle of Latanoprost eye
drops with no date opened or expiration date, one unopened Latanoprost eye drops with pharmacy
instructions to refrigerate until opened, and two unopened insulin glargine pens with pharmacy instructions
to refrigerate until opened.
During an interview on [DATE] at 8:45 AM, Staff C, LPN, stated, We should not have the unopened eye
drops or insulin on the cart. We should date them when we get them. All insulin and eye drops should have
dates on them.
During an observation of Medication Cart #3 on [DATE] at 8:55 AM with Staff D, Registered Nurse (RN),
there were one opened Lispro insulin with no date opened or expiration date, one unopened Lantus insulin
with pharmacy instructions to refrigerate until opened, one opened Lantus insulin with no date opened or
expiration date, and one opened Lispro insulin with an expiration date of [DATE].
During an interview on [DATE] at 9:05 AM, Staff D, RN, stated, All insulin should be labeled with the date
opened or when they expire. We should not have the insulin that is expired on the cart, and we should keep
the insulin in the refrigerator until we need to use it.
During an observation of Medication Cart #4 on [DATE] at 9:12 AM with Staff E, LPN, there were one
unlabeled, undated medication cup with eleven pills, one opened Basaglar insulin with no date opened or
expiration date, and one opened insulin glargine with an expiration date of [DATE] and pharmacy
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 8 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
instruction to use within 28 days.
Level of Harm - Minimal harm
or potential for actual harm
During an interview on [DATE] at 9:20 AM, Staff E, LPN, stated, I should not pre-pour medications. The
expired insulin should not be on the cart. I didn't know it was there. All insulins should be labeled when
opened and when it expires.
Residents Affected - Many
During an interview on [DATE] at 7:50 AM, the Director of Nursing (DON) stated, No medications should
ever be pre-poured. Insulin should be dated and if expired taken off the cart. Insulin and eye drops that
need to be kept in the refrigerator, should be kept there.
Review of the facility policy and procedure titled 6.0 General Dose Preparation and Medication
Administration with the last revision date of [DATE] and the last approval date of [DATE] read, Applicability:
The Policy 6.0 sets forth the procedures relating to general dose preparation and medication
administration. Facility staff should also refer to Facility policy regarding medication administration and
should comply with Applicable Law and the State Operations Manual when administering medications.
Procedure . 3. Dose Preparation: Facility should take all measures required by Facility policy and Applicable
Law, including, but not limited to the following . 3.10 Facility staff shall not leave medications or chemicals
unattended . 3.12. Facility staff should enter the date opened on the label of the medications with shortened
expiration dates (e.g., insulins, irrigation solutions, etc.) . 7. Facility should ensure that medication carts are
always locked when out of sight or unattended.
Review of the facility policy and procedures titled 5.3 Storage and Expiration Dating of Medications,
Biologicals with the last approval date [DATE] read, Applicability: This Policy 5.3 sets forth the procedures
relating to the storage and expiration dates of medications, biologicals, syringes, and needles. Procedure .
4. Facility should ensure that medications and biologicals that are: (1) have an expiration date on the label,
(2) have been retained longer than recommended by manufacturer or supplier guidelines; or (3) have been
contaminated or deteriorated, are stored separate from other medications until destroyed or returned to the
pharmacy or supplier. 5. Once any medication or biological package is opened, Facility should follow
manufacturer/supplier guidelines with respect to expiration dates for opened medications. Facility staff
should record the date opened on the primary medication container (vial, bottle, inhaler) when the
medication has a shortened expiration date once opened or opened. 5.1 Facility staff may record the
calculated expiration date based on date opened on the primary medication container . 5.4 When an
ophthalmic solution or suspension has a manufacturers shortened beyond use date once opened, facility
staff should record the date opened and the date to expire on the container . 10. Facility should ensure that
medications and biologicals are stored at their appropriate temperatures according to the United States
Pharmacopeia guidelines for temperature ranges. Facility staff should monitor the temperature of vaccines
twice a day . 10.2 Refrigeration 36° to 46° F or 2° to 8°C.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 9 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
Based on observation, interview, and record review, the facility failed to ensure food was safely and
properly stored and labeled in the areas of kitchen reach-in cooler, and the reach-in, and walk-in freezer,
failed to ensure the kitchen equipment were kept clean, and failed to ensure dietary staff had hair covering
while in the kitchen area.
Findings include:
During an observation while conducting a walk-through tour of the kitchen with the Charge [NAME] on
3/17/2024 at 9:02 AM, the Charge [NAME] and Staff A, Dietary Aide, had no hair covering. There were
several containers of unidentifiable food items in the reach-in cooler without an identifying label or date.
There were several items including a large metal mixing bowl partially covered with contents spilling out
onto other items, a tray with six individual dessert type food, and an open plastic bag of egg type product in
the reach-in freezer without an identifying label or date. There was a large buildup of ice around the door
and on the ice curtain of the walk-in freezer. There were several boxes remaining on the floor of the walk-in
freezer.
During an interview on 3/17/2024 at 9:15 AM, the Charge [NAME] confirmed that the items in the reach-in
cooler and reach-in freezer did not have an identifying label or date and should have been labelled and
dated before storing. The Charge [NAME] confirmed the items on the floor of the freezer and the ice buildup
around the door and on the ice curtain and stated it was due to the door not being closed properly. The
Charge [NAME] stated the truck delivery date was on Tuesdays and the food should have been put away
and not left remaining on the floor of the freezer. The Charge [NAME] confirmed that she and Staff A were
not wearing proper hair covering.
During an interview on 3/17/2024 at 9:16 AM, Staff A, Dietary Aide confirmed he was not wearing a hairnet
or a beard guard.
During the follow up tour of the kitchen on 3/18/2024 at 5:45 AM, there were food items already placed on
the tray line at 5:49 AM. There was a large buildup of food bits and dried debris on the countertop can
opener.
During an interview on 3/18/2024 at 5:50 AM, the Charge [NAME] stated that she had placed the food on
the tray too early and should not be there until 30 minutes prior to tray service.
During an interview on 3/18/2024 at 8:42 AM, the Certified Dietary Manager (CDM) stated it was her
expectation that all policies and training were followed. The CDM stated that all dietary staff were required
to wear hair coverings while working in the department. The CDM stated it was her expectation that all
leftover foods were labelled and dated before being stored. The CDM stated that the equipment, including
the can opener, should be cleaned daily.
Review of the facility policy and procedures titled Personal Appearance last reviewed on 3/19/2024, read, 3.
Hair cover is to be worn by any/all staff working with food in the kitchen.
Review of the facility policy and procedures titled Food Storage dated October 1, 2019 and last reviewed on
3/19/2024, read, Procedure . 2. Refrigerators . d. Date, label, and tightly seal all refrigerated foods using
clean, nonabsorbent, covered containers that are approved for food storage . 3.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 10 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
Freezers . c. Store all foods on racks or shelves off the floor . e. Store frozen foods in moisture-proof wrap or
containers that are labeled and dated.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 11 of 12
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105308
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avante at Inverness Inc
304 S Citrus Ave
Inverness, FL 34452
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and record review, the facility failed to ensure staff performed hand
hygiene during medication administration to prevent from possible spread of infection and communicable
diseases in 3 of 4 medication administration observations.
Residents Affected - Few
Findings include:
During an observation on 3/19/2024 at 8:50 AM, Staff J, Licensed Practical Nurse (LPN), returned to the
medication cart after administering medications to a resident. Without performing hand hygiene, Staff J
prepared Resident #34's medications and administered the medications to the resident. At 9:01 AM, Staff J
returned to the medication cart, prepared Resident #10's medications, and administered the medications to
the resident. At 9:04 AM, Staff J returned to the medication cart. Staff J prepared Resident #11's
medications and administered the medications.
During an interview on 3/19/2024 at 9:15 AM, Staff J, LPN, stated, I should have used hand sanitizer before
and after getting the meds to the residents. I don't know why I didn't.
During an interview on 3/19/2024 at 2:15 PM, the Director of Nursing (DON) stated, All medication policies
should be followed. Hand washing should be done with all medication administration and staff should follow
policies and procedures.
Review of the facility policy and procedure titled 6.0 General Dose Preparation and Medication
Administration with the last revision date of 1/1/2022 and the last approval date of 12/29/2023 read,
Applicability: The Policy 6.0 sets forth the procedures relating to general dose preparation and medication
administration. Facility staff should also refer to Facility policy regarding medication administration and
should comply with Applicable Law and the State Operations Manual when administering medications.
Procedure . 2. Prior to preparing or administering medications, authorized and competent Facility staff
should follow Facility's infection control policy (e.g., hand washing).
Review of the facility policy and procedures titled Hand Hygiene with the last approval date of 12/29/2023
read, Policy: This facility considers hand hygiene the primary means to prevent the spread of infections.
Procedure . 2. All personnel shall follow the handwashing/hand hygiene procedures to help prevent the
spread of infections to other personnel, residents, and visitors . 5. Use an alcohol-based hand rub
containing at least 62% alcohol; or, alternatively, soap (antimicrobial or non-antimicrobial) and water for the
following situations . c. Before preparing or handling medications.
Review of the facility policy and procedures titled Infection Control- Medication Administration with the last
approval date of 12/29/2023 read, Policy: It is the policy of the facility to ensure that appropriate infection
prevention and control measures are taken to prevent the spread of infection in accordance with State and
Federal regulations, and national guidelines. Procedure: 1. Hand hygiene is performed prior to handling any
medication.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105308
If continuation sheet
Page 12 of 12