Device recall
Z-0739-2022: Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone…
FDA device recall · Class II · Nextremity Solutions
Key facts
| Recall number (Z-number) | Z-0739-2022 |
|---|---|
| Recall event | 89588 |
| Product | Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT |
| Product code | HWC |
| Recalling firm | Nextremity Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 24, 2024 |
| 510(k) numbers | K200840, K213530 |
| 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