Device recall
Z-2422-2018: AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10…
FDA device recall · Class II · Cayenne Medical Inc.
Key facts
| Recall number (Z-number) | Z-2422-2018 |
|---|---|
| Recall event | 80282 |
| Product | AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm). For orthopedic use in ligament reconstruction. |
| Product code | HWC |
| Recalling firm | Cayenne Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 14, 2018 |
| 510(k) numbers | K083612 |
| FEI number | 3006108336 |
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