Device recall
Z-0625-2021: PHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0625-2021 |
|---|---|
| Recall event | 86896 |
| Product | PHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042, 14-405044, 14-405070 - Product Usage: Fracture fixation of small bones, small bone fragements and long bones. |
| Product code | HSB |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2024 |
| 510(k) numbers | K063570 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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