Device recall
Z-0925-2021: Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with…
FDA device recall · Class I · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-0925-2021 |
|---|---|
| Recall event | 87053 |
| Product | Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal SlingBar 350 R2R (product… |
| Product code | FSA |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 26, 2023 |
| FEI number | 1824206 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database