Device recall
Z-2242-2021: smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during…
FDA device recall · Class II · Smith & Nephew Orthopaedics Ltd. (Aurora)
Key facts
| Recall number (Z-number) | Z-2242-2021 |
|---|---|
| Recall event | 88311 |
| Product | smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during orthopedic surgery. |
| Product code | NXT |
| Recalling firm | Smith & Nephew Orthopaedics Ltd. (Aurora) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 13, 2024 |
| PMA numbers | P040033 |
| FEI number | 3005975929 |
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