Recall Z-0640-2022— Hill-Rom, Inc.

Name: FDA recall Z-0640-2022
Creator: U.S. Food and Drug Administration
Published: 2021-12-23

Class II · Ongoing

Class II FDA medical device recall by Hill-Rom, Inc., initiated 2021-12-23. FDA's recall record names no specific 510(k) clearance for this event. Product: Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015. Reason: Missing bushing on Liko M220 and M230 causing wear and potential for patient falling.

Recalling firm: Hill-Rom, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2021-12-23
Firm location: Batesville, IN, United States

Product description

Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015

Reason for recall

Missing bushing on Liko M220 and M230 causing wear and potential for patient falling

Data sourced from openFDA. This site is unofficial and independent of the FDA.