Device recall
Z-0618-2011: Stryker Titanium Intraline Anchor, Model Numbers 3910400050, 3910400055…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-0618-2011 |
|---|---|
| Recall event | 53182 |
| Product | Stryker Titanium Intraline Anchor, Model Numbers 3910400050, 3910400055, 3910400060, 3910400065, Soft Eyelet Anchor, manufactured by Stryker Endoscopy, Puerto Rico |
| Product code | HWC |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 14, 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