Device recall
Z-2321-2016: TWIST DR 25X95MM Cann 12MM Thd 30MM AO; The twist drill is used to drill holes…
FDA device recall · Class II · Zimmer Gmbh
Key facts
| Recall number (Z-number) | Z-2321-2016 |
|---|---|
| Recall event | 74548 |
| Product | TWIST DR 25X95MM Cann 12MM Thd 30MM AO; The twist drill is used to drill holes into bones/tissues for foot, ankle and hand implant systems. |
| Product code | LXH |
| Recalling firm | Zimmer Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 30, 2017 |
| FEI number | 3005233524 |
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