Incomplete Infection Prevention Program and Medication Administration Breaks
Summary
The facility failed to establish and maintain a comprehensive, facility-specific infection prevention and control program for Legionella and other water-borne pathogens. The Water Management Program policy, last revised 10/12/23, did not include a CDC toolkit assessment with control measures such as physical controls, temperature management, disinfectant level control, visual inspections, or environmental testing for pathogens. A completed CDC Legionella Environmental Assessment Form was missing, and there was no facility-specific infection prevention program or plan to address outbreaks of Legionella or other water-borne pathogens. The policy also stated the program would be reviewed annually, while the document metadata listed the next review as 10/12/26. The facility had a sprinkler system supplied by the local water company, a sprinkler riser room serving the whole facility, mop/service sinks, water heaters, resident room sinks and bathrooms, bathhouses, dining room sinks, ice machines, and steam tables throughout the building. The facility also failed to ensure appropriate hand hygiene and infection control practices during medication administration. One resident had diagnoses of DM II with hyperglycemia and CKD stage 5 and was ordered Refresh Tears ophthalmic solution. During medication administration, a CMT sanitized hands, entered the room, put on gloves, administered oral medications, and then gave the eye drops with the same gloved hands before removing gloves. Another resident with Parkinson's disease was ordered an Aspercreme Lidocaine patch. During medication administration, the same CMT sanitized hands, prepared the medication, put on gloves, administered oral medications, and then applied the patch with the same gloved hands before removing gloves and sanitizing hands. Staff interviews confirmed the CMT did not perform hand hygiene correctly and should have removed gloves, sanitized hands, and put on new gloves between different routes of administration. The facility further failed to follow its insulin injection procedure for another resident with DM II who was ordered Insulin Lispro Junior KwikPen 10 units with meals. During observation, an LPN removed the cap from the insulin pen, did not wipe the rubber seal with alcohol, attached a needle, dialed the dose, and administered the insulin. The facility policy required the rubber cap to be swabbed with alcohol before attaching the needle. The LPN acknowledged not wiping the seal and stated it was because he/she was nervous while being observed. In addition, the facility's infection control surveillance logs were incomplete and did not contain the required monthly tracking, antibiotic reports, lab or X-ray results, or other documentation across multiple units and months. The IP stated the tracking material was what the prior IP had left and knew it was incomplete, while the DON stated the infection tracking book should have included maps, required reports, monitoring criteria, lab and X-ray results, antibiotic lists, and education when trends were identified.
Penalty
Resources
Below are regulatory guidelines relevant to this citation:
Trusted data from CMS and state health departments
Every citation, penalty and Plan of Correction is sourced from public CMS records (latest release July 29, 2026) and official state health department websites — never guesswork.
In your survey window? See what surveyors are citing.
The Survey-Prep Report maps your facility's risk from 12 months of CMS and state citation data — what's being cited around you and what to check first. $129 one-time.