Hill-Rom, Inc. recalls Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
- Recall date
- December 23, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0640-2022
- FDA classification
- Class II
- Brand / firm
- Hill-Rom, Inc.
- Sold / distributed
- Worldwide distribution - US Nationwide and the countries of Austria, Austria, Bahrain, Canada, Switzerland, Germany, Denmark, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Israel, Italy, Norway, Saudi Arabia, Sweden, Slovenia, Taiwan (Province of China), South Africa, Oman.
Why it was recalled
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
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