Device recall
Z-1458-2020: Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile…
FDA device recall · Class II · Nextremity Solutions
Key facts
| Recall number (Z-number) | Z-1458-2020 |
|---|---|
| Recall event | 84924 |
| Product | Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra Hammertoe Correction System is a system of implants and associated instruments which is indicated for small bone reconstruction limited to inter-digital repair and fusion of the… |
| Product code | HWC |
| Recalling firm | Nextremity Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 17, 2020 |
| 510(k) numbers | K110445 |
| FEI number | 3009540749 |
At a glance
- 1–9 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