FDA Device recall Z-0639-2022
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
- FDA Device
- Class II
- ongoing
- Published 2022-02-23
On 2022-02-23 the FDA classified a Class II recall of Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010 by Hill Rom, citing missing bushing on Liko M220 and M230 causing wear and potential for patient falling.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0639-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-12-23 |
| Published | 2022-02-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Hill Rom |
| Distribution | US |
Product
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Reason
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
Identifiers
| code_info | Serial numbers: 5263715-5269464. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
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FDA Device · Class II · 2022-03-23 · Hill Rom - Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
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FDA Device · Class II · 2021-12-29 · Hill Rom - LikoStretch 1900 Model Number: 3156051 - The combination of this products allows the user to easily adjust/control the center of gravity du…
FDA Device · Class II · 2021-10-06 · Hill Rom - OctoStretch with Stretch Leveller - The combination of this products allows the user to easily adjust/control the center of gravity during…
FDA Device · Class II · 2021-10-06 · Hill Rom
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0639-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.