Use cautionMedical device recall · FDA · Published December 23, 2021
Hill-Rom Liko Mobile Lifts Recall: Missing Bushing Risk of Patient Falling
Hill-Rom recalls Liko M230 lifts (model 2050015) sold 2016-2021 with missing bushing causing patient falls. Affected units have serial numbers 5361393-5362761. Contact Hill-Rom for remedy.
“Hill-Rom Liko Mobile Lifts Recall: Missing Bushing Risk of Patient Falling.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61341-hill-rom-liko-mobile-lifts-recall-missing-bushing-risk-of. Based on FDA recall #Z-0640-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0640-2022%22&limit=1).
The FDA announced on Dec. 23, 2021, that Hill-Rom, Inc. is recalling Liko Mobile Lifts due to a missing bushing hazard. The agency said the defect causes wear and potential for patient falling.
How to tell if you have it
Brand: Hill-Rom
Product: LikoM230 Model: 2050015
Serial numbers: 5361393-5362761
Manufactured between 2016-DEC-27 and 2021-SEP-01
UDI: 0887761GMN000034U5
The hazard
The recall involves a missing bushing on Liko M220 and M230 models. This defect causes wear and creates the potential for patient falling.
Context
GovInfoNow's records show Hill-Rom, Inc. has 9 other recalls on record since 2018-01-12. Other recent recalls of similar products include WHILL Recalls Wheelchairs Due to Brake Failure Risk (2025-12-29), Arjo Tenor Patient Lift Recall: Risk of Uncontrolled Drop (2026-03-10), and Mirion Captus 4000e Thyroid Uptake System Recall: Tension Bolt Failure Risk (2026-07-20).
How to tell if you have this one
Check for serial numbers starting with 5361393 and ending with 5362761. The lifts were manufactured between December 2016 and September 2021.
Brand
Hill-Rom
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
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.
Recall number
Product, codes & lots
Quantity
Z-0639-2022
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010; Serial numbers: 5263715-5269464. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5
5470 units
Z-0640-2022
Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015; Serial numbers: 5361393-5362761. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5
1215 units
Based on the official FDA remedy
What to do — step by step
Check Serial Numbers
Look for serial numbers in the range 5361393-5362761 on the lift.
Contact Hill-Rom
Reach out to Hill-Rom for instructions on how to fix or replace the lift.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0640-2022 (December 23, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0640-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.