Liko Mobile Lifts: Primarily intended for use in nursing homes Liko… — Class II medical device recall Z-0639-2022
Ongoing recall by Hill-Rom, Inc., reported 2022-02-23, distributed nationwide. Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
| Recall number | Z-0639-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom, Inc., Batesville, IN, United States |
| Recall initiated | 2021-12-23 |
| Classified | 2022-02-14 |
| Reported by FDA | 2022-02-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BH, CA, CH, CN, DE, DK, ES, FI, FR, GB, GR, HK, IE, IL, IT, NO, OM, SA, SE, SI, TW, ZA |
| Quantity | 5,470 units |
| Serial numbers | 5263715-5269464 |
| Model numbers | 2050010 |
Product
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Reason for recall
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0639-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.