Device recall
Z-0105-2019: Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient…
FDA device recall · Class II · Liko AB
Key facts
| Recall number (Z-number) | Z-0105-2019 |
|---|---|
| Recall event | 80911 |
| Product | Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations. |
| Product code | FSA |
| Recalling firm | Liko AB |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2019 |
| FEI number | 6884 |
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