FDA Device recall Z-0640-2022
Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
- 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 LikoM230 Model: 2050015 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-0640-2022 |
| 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 LikoM230 Model: 2050015
Reason
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
Identifiers
| code_info | Serial numbers: 5361393-5362761. 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.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0640-2022%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.