[Recalled] Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015 — Missing bushing on Liko M220 and M230 causing wear and potential for patient fa… | FDA 2021-12-23
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015 |
|---|---|
| Brand / manufacturer | Hill-Rom, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0640-2022 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 23 December 2021 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Hill-Rom, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.