Device recall
Z-2470-2021: Arjo Disposable Repositioning Sling, Model AHD001
FDA device recall · Class II · Getinge Dominican Republic SA
Key facts
| Recall number (Z-number) | Z-2470-2021 |
|---|---|
| Recall event | 88403 |
| Product | Arjo Disposable Repositioning Sling, Model AHD001 |
| Product code | FSA |
| Recalling firm | Getinge Dominican Republic SA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2023 |
| FEI number | 3012292104 |
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