Device recall
Z-1635-2016: CinchLock Flex Knotless Anchor with Inserter; Model number CAT02643; Orthopedic…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1635-2016 |
|---|---|
| Recall event | 73846 |
| Product | CinchLock Flex Knotless Anchor with Inserter; Model number CAT02643; Orthopedic: The Pivot CinchLock SS Knotless Anchor (CAT02462) and Pivot CinchLock Flex Knotless Anchor (CAT02463) are non-degradable implant devices intended for the fixation of soft tissue to bone. Used for repair of hip… |
| Product code | MBI |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 12, 2016 |
| 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