Infection Control Failures During Resident Care and Equipment Handling
Summary
The facility failed to ensure infection prevention and control practices were followed during multiple resident care activities and equipment handling. The report states that Hoyer lifts were used for transfers without being disinfected before or after use. On one occasion, staff brought the lift into Resident 7’s room without disinfecting it, used it to transfer the resident from a wheelchair to bed, and then placed it back in the hallway without cleaning it. The same lift was later taken into another resident’s room and used again without disinfection. An RN and NA confirmed the lift had not been disinfected before or after use, and the DON confirmed staff should have disinfected it. The facility also failed to follow barrier precautions and hand hygiene expectations during care for a resident in EBP. Resident 14 had an ileostomy and PEG tube and was identified in the care plan as requiring gowns and gloves during high-contact care. During PEG tube care, an RN performed hand hygiene and gloved but did not wear a gown. During ileostomy care, an NA performed the task with gloves but without a gown. The RN confirmed the resident was in EBP and that both staff members should have worn gowns during those cares. Additional infection control failures involved respiratory equipment and linen handling. Resident 7’s nebulizer administration kit was observed multiple times with residual liquid remaining in it, and staff did not rinse the kit after use as required by facility policy. During incontinence and hygiene care for Resident 3, an NA removed soiled briefs, performed perineal care, removed gloves, and reapplied new gloves without hand hygiene. The same NA also placed washcloths on the bedside table without a barrier and squeezed washcloths against the sink basin before using them for facial and perineal care; both the NA and RN confirmed these actions could cause cross contamination. For Resident 9, respiratory equipment was observed stored and maintained without required labeling or proper placement. The resident had orders for oxygen, BiPAP with heated humidification, and nebulizer treatment. The nebulizer kit and tubing were undated, the disposable oxygen humidification bottle was undated, the BiPAP bleed-in tubing was stored on the floor, and the BiPAP mask was left on the bedside table without a barrier. The LPN and the ADON/Infection Preventionist confirmed these items should have been dated and stored in a manner to prevent cross-contamination.
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