Device recall
Z-1675-2020: aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
FDA device recall · Class II · AAP Implantate Ag
Key facts
| Recall number (Z-number) | Z-1675-2020 |
|---|---|
| Recall event | 84716 |
| Product | aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00 |
| Product code | GAD |
| Recalling firm | AAP Implantate Ag |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 27, 2025 |
| FEI number | 3001406084 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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