Device recall
Z-1500-2021: InCore Lapidus Disposable Kit 28mm Left, Part Number: IC-LAP-28L - Product…
FDA device recall · Class II · Nextremity Solutions
Key facts
| Recall number (Z-number) | Z-1500-2021 |
|---|---|
| Recall event | 87665 |
| Product | InCore Lapidus Disposable Kit 28mm Left, Part Number: IC-LAP-28L - Product Usage: Intended as a three-part construct intended for internal fixation for First Metatarsocuneiform arthrodesis. |
| Product code | HWC |
| Recalling firm | Nextremity Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 10, 2021 |
| FEI number | 3009540749 |
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