Device recall
Z-0096-2021: SwiftHook sold as the following: a. Individually as SwiftHook b. Included with…
FDA device recall · Class II · Handicare AB
Key facts
| Recall number (Z-number) | Z-0096-2021 |
|---|---|
| Recall event | 86318 |
| Product | SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage: The mobile lifts are intended to assist people with functional impairments in scenarios involving physical positioning. |
| Product code | FSA |
| Recalling firm | Handicare AB |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 30, 2023 |
| FEI number | 3009481053 |
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