Device recall
Z-2534-2020: DUFNER Instrumente GmbH-De Bakey Slim Needleholder- intended to hold a suturing…
FDA device recall · Class II · Dufner Instrumente GmbH
Key facts
| Recall number (Z-number) | Z-2534-2020 |
|---|---|
| Recall event | 85894 |
| Product | DUFNER Instrumente GmbH-De Bakey Slim Needleholder- intended to hold a suturing needle for closing wounds during suturing and surgical procedures Reference Number: 18044-23 |
| Product code | FHQ |
| Recalling firm | Dufner Instrumente GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 21, 2021 |
| FEI number | 3002806862 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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