Device recall
Z-1533-2008: Stryker Peek Intraline Anchor, 5.5 mm, Model number 3910-400-010 Used for tissue…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-1533-2008 |
|---|---|
| Recall event | 46916 |
| Product | Stryker Peek Intraline Anchor, 5.5 mm, Model number 3910-400-010 Used for tissue fixation to bone in certain areas. |
| Product code | HWC |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2010 |
| 510(k) numbers | K071157 |
| 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