Device recall
Z-1328-2025: Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1328-2025 |
|---|---|
| Recall event | 96281 |
| Product | Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197 |
| Product code | MBI |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K151314 |
| FEI number | 2936485 |
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