F 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record view, the facility failed to develop a person-centered care plan for 1 of 3 residents
reviewed for respiratory services, Resident #43.
Findings include:
Review of Resident #43's physician order dated 10/17/2023 reads, Apply Oxygen @ [at] 2 liters via nasal
cannula for SOB [shortness of breath] or sats <90% [saturation less than 90 percent].
Review of Resident #43's Weights and Vital Summary reads, 11/21/2023 00:56 [12:56 AM] 93% (Oxygen
via Nasal Cannula) . 11/17/2023 16:01 [4:01 PM] 98% (Oxygen via Nasal Cannula) . 11/06/2023 19:45
[7:45 PM] 96% (Oxygen via Nasal Cannula) . 11/04/2023 23:30 [1:30 PM] 95% (Oxygen via Nasal
Cannula).
Review of Resident #43's Minimum Data Set, dated [DATE] showed the resident uses oxygen while a
resident.
Review of Resident #43's care plan did not reveal a focus for shortness of breath or oxygen therapy.
During an interview on 11/29/2023 at 2:00 PM, the Director of Nursing stated, Our practice is to develop
care plans based on residents' needs. [Resident #43's name] had a physician order and there is
documentation that oxygen was administered. There should have been a focus in her care plan regarding
oxygen, but I do not see one.
Review of the facility policy and procedures titled Comprehensive Care Plans with the last review date of
1/30/2023 reads, Policy: It is this policy of this facility to develop and implement a comprehensive
person-centered care plan for each resident, consistent with resident rights, that includes measurable
objectives and timeframes to meet a resident's medical, nursing, and mental and psychosocial needs that
are identified in the resident's comprehensive assessment.
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 5
Event ID:
106066
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
106066
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/30/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Oak Hammock at the University of Florida Inc
2660 SW 53rd LN
Gainesville, FL 32608
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 0658
Ensure services provided by the nursing facility meet professional standards of quality.
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 accepted professional standards of
practice were followed for intravenous medication administration via midline catheter for 1 of 3 residents
with midline catheters, Resident #52.
Residents Affected - Few
Findings include:
Review of Resident #52's admission record showed the resident was admitted on [DATE] with the
diagnoses including sepsis, tubo-ovarian abscess (a pocket of pus due to infection of the ovary and
fallopian tube), pelvic inflammatory disease, peritoneal abscess, chronic obstructive pulmonary disease,
essential primary hypertension, hyperlipidemia, iron deficiency anemia, primary osteoarthritis, and
presence of artificial hip joint.
Review of Resident #52's physician orders dated 11/4/2023 reads, Piperacillin Sod-Tazobactam So
Solution Reconstituted 3-0.375 GM (grams), Use 3.375 gm intravenously four times a day for sepsis w/o
[without] acute organ dysfunction/tubo ovarian abscess until 12/07/2023 06:59 [6:59 AM], Administer every
6 hours at 10am, 4 pm, 10pm, 4 am.
Review of Resident #52's physician order dated 11/4/2023 reads, Flush midline using SASH method
[Saline-ABT [Antibiotic]-Saline-Heparin) with each IV [Intravenous] ABT administration, four times a day for
IV ABT.
During an observation of medication administration on 11/27/2023 at 11:00 AM, Staff C, Licensed Practical
Nurse (LPN), assembled all supplies for intravenous antibiotic administration for Resident # 52 without
performing hand hygiene. Staff C, LPN, removed the end cap of the intravenous tubing and attached the
antibiotic bag to the intravenous line. Staff C removed the end cap of the intravenous tubing and attached
the antibiotic bag to the intravenous line. Staff C held the uncapped end of the intravenous tubing in her left
hand and cleansed the needleless hub of the midline catheter with alcohol with right hand for less than 2
seconds. Staff C did not allow the needleless hub to dry before attaching a 10-milliliter normal saline flush.
Without observing the insertion site or attempting to verify for blood return, Staff C administered the normal
saline and the antibiotic.
During an interview on 11/27/2023 at 11:07 AM, Staff C, LPN, stated, I did not verify for blood return prior
to hanging the medicine. I should have cleaned the needleless connector longer and let it dry before giving
the flush or antibiotic.
During an interview on 11/29/2023 at 1:00 PM, the Director of Nursing (DON) stated, Staff should attempt
to verify midline placement and clean the needleless connector before giving antibiotics. They should follow
our procedures.
Review of the facility policy and procedures titled Intermittent infusion device flushing and locking with the
last revision date of 8/21/2023 reads, Introduction: An intermittent infusion device consists of an IV catheter
with a needleless connector attached. This device helps maintain venous access in a patient who receives
IV medications or solutions intermittently or in a patient who might need medications should an emergency
arise. An intermittent flush device requires flushing before each infusion to assess vascular access device
function, after each infusion to prevent mixing of incompatible medications and solutions, and after blood
sampling to clear the device of blood and debris .
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106066
If continuation sheet
Page 2 of 5
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
106066
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/30/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Oak Hammock at the University of Florida Inc
2660 SW 53rd LN
Gainesville, FL 32608
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 0658
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Hospital-acquired condition alert: Keep in mind that the Centers for Medicare and Medicaid Services
considers vascular catheter-associated infection a hospital acquired condition because it can reasonably
[be] prevented using a variety of best practices. Make sure to follow evidence-based infection prevention
practices, such as performing hand hygiene, using sterile no-touch technique, and performing a vigorous
mechanical scrub of needleless connectors to reduce the risk of vascular catheter-associated infections .
Implementation . Assess the intermittent infusion device insertion site to ensure that it's free from signs of
infection, infiltration, and phlebitis . Perform a vigorous mechanical scrub of the needleless connector for at
least 5 seconds using an antiseptic pad. Allow it to dry completely. While maintaining sterility of the syringe
tip, attach a prefilled 10-ml [milliliter] syringe or a syringe designed to generate lower injection pressure
containing preservative-free normal saline solution to the needleless connector. Unclamp the intermittent
infusion device and aspirate slowly for a blood return that's the color and consistency of whole blood.
Review of the facility policy and procedures titled Medication Administration with the last revision date of
2/27/2023 reads, Policy: Medications are administered by licensed nurses, as ordered by the physician and
in accordance with professional standards of practice, in a manner to prevent contamination or infection.
Policy Explanation and Compliance Guidelines . 4. Wash hands prior to administering medication per facility
protocol and product.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106066
If continuation sheet
Page 3 of 5
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
106066
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/30/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Oak Hammock at the University of Florida Inc
2660 SW 53rd LN
Gainesville, FL 32608
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 - Some
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.
Based on observation, interview, and record review, the facility failed to ensure that all drugs and
biologicals used in the facility were stored and labeled in accordance with currently accepted professional
standards and included expirations dates when applicable in 2 of 4 medication carts reviewed.
Findings include:
During an observation of Medication Cart 1 on 11/27/2023 at 9:15 AM with Staff A, Licensed Practical
Nurse (LPN), there were one 30-milliliter medication cup with chocolate pudding and crushed pieces of
medications with no label identifying the medication or any resident identifier, one opened bottle of
Brimonidine/ timolol ophthalmic solution with no opened or expiration dates, and one opened Basaglar
insulin pen with no opened or expiration dates.
During an interview on 11/27/2023 at 9:25 AM, Staff A, LPN, stated, That cup of medications with the
pudding is for a resident who refused the medications earlier and I was going to go back and check before I
threw it out. I should have labeled who it was for and what medications were in it. The eye drops and insulin
should have a date they were opened.
During an observation of Medication Cart 2 on 11/27/2023 at 9:30 AM with Staff B, LPN, there were one
30-milliliter medication cup with chocolate pudding with pieces of crushed medications with no label
identifying the medications or any resident identifier, one medication cup that contained two medications
(one red capsule and one white tablet) with no label identifying the medications and no resident identifier,
one medication cup with three medications (2 white tablets and 1 yellow tablet) with no label identifying the
medications and no resident identifier, one medication cup with four tablets brown in color with no label
identifying the medication and no resident identifier, one opened bottle of Polymycin B and trimethoprim
ophthalmic solution with no opened or expiration dates, one opened bottle of Brimonidine ophthalmic
solution with no opened or expiration dates, one opened bottle of Systane eye drops with no opened or
expiration dates, and one opened bottle of Bimatoprost ophthalmic solution with no opened or expiration
dates.
During an interview on 11/27/2023 at 9:40 AM, Staff B, LPN, stated, I was just called away to help a
resident and didn't get to give these medicines. I should have given them. They should be labeled with what
the medications are and who they are for. I didn't have Vitamin B Complex, so I borrowed these from
another nurse. There is no label as what they are. All eye drops should be labeled with the date they are
opened or when they expire.
During an interview on 11/29/2023 at 1:00 PM, the Director of Nursing (DON) stated, The nurses should
administer the medications when they get them ready. They should have gotten a new bottle of Vitamin B
Complex and not borrowed from another cart and put them in her cart. All medications should have the
date opened or expiration dates on them.
Review of the facility policy and procedures dated 2/27/2023 reads, Policy: It is the policy of this facility to
ensure all medications housed on our premises will be stored in the pharmacy and/or medication rooms
according to manufacturer's recommendations and sufficient to ensure proper sanitation, temperature, light,
ventilation, moist control, segregation and security.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106066
If continuation sheet
Page 4 of 5
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
106066
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/30/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Oak Hammock at the University of Florida Inc
2660 SW 53rd LN
Gainesville, FL 32608
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 intravenous medication administration.
Residents Affected - Some
Findings include:
During an observation of medication administration on 11/27/2023 at 10:45 AM, Staff C, Licensed Practical
Nurse (LPN), prepared medications for Resident #167 without performing hand hygiene, entered the
resident's room and administered the medications. Staff C exited the room and went to the medication cart
to prepare medications for another resident.
During an observation of medication administration on 11/27/2023 at 11:00 AM, Staff C, LPN, prepared
medications for Resident #52 without performing hand hygiene, entered the resident's room and
administered the oral medications without performing hand hygiene. Staff C donned gloves and placed
gloved hands inside the rim of the trash can and moved the trash can closer. Staff C then picked up the bag
of antibiotics and intravenous tubing, removed the end cap of the intravenous tubing and attached the
antibiotic bag to the intravenous line. Staff C held the uncapped end of the intravenous tubing in her left
hand and cleansed the hub of the midline catheter with alcohol with right hand for less than 2 seconds. The
uncapped end of the intravenous tubing was touching the sheets on the bed and the resident's arm. Staff C
attached the intravenous tubing to the midline catheter, removed gloves, and exited the room without
performing hand hygiene.
During an interview conducted on 11/27/2023 at 11:07 AM, Staff C, LPN, stated, I did not wash my hands
before preparing the medications. I reached into the trash can with my gloved hands. I should have
changed my gloves after that. I didn't realize that the end of the IV line touched the resident or the sheets.
During an interview on 11/29/2023 at 1:00 PM, the Director of Nursing (DON) stated, All staff should
practice infection control standards and wash their hands before and after administering medications.
Review of the facility policy and procedures titled Medication Administration with the last revision date of
2/27/2023 reads, Policy: Medications are administered by licensed nurses, as ordered by the physician and
in accordance with professional standards of practice, in a manner to prevent contamination or infection.
Policy Explanation and Compliance Guidelines . 4. Wash hands prior to administering medication per facility
protocol and product.
Review of the facility policy and procedures titled Hand Hygiene with the approval date of 1/30/2023 reads,
Purpose: To ensure that all staff perform proper hand hygiene procedures to prevent the spread of infection
to other personnel, residents and visitors. Policy Explanation and Compliance Guidelines: 1. Staff will
perform hand hygiene when indicated, using proper technique consistent with accepted standards of
practice.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106066
If continuation sheet
Page 5 of 5