Device recall
Z-1239-2007: Stryker Radius Locking Caps, Catalog Number: 486610000, Manufactured by Stryker…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-1239-2007 |
|---|---|
| Recall event | 38406 |
| Product | Stryker Radius Locking Caps, Catalog Number: 486610000, Manufactured by Stryker Spine SAS Z.I. Marticot - 33610 Cestas France.,Distributed by Howmedica Osteonics Corp. 325 Corporate Drive, Mahway, NJ 07430 |
| Product code | NKB |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 11, 2007 |
| 510(k) numbers | K062270 |
| FEI number | 3004024955 |
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