Device recall
Z-0868-2009: Dri-Lok Disposable Cannula, Part numbers 3910-075-500, 3910-075-501…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-0868-2009 |
|---|---|
| Recall event | 50525 |
| Product | Dri-Lok Disposable Cannula, Part numbers 3910-075-500, 3910-075-501, 3910-075-502, 3910-075-650, 3910-075-651, 3910-075-652, 3910-075-800, 3910-075-801, 3910-075-802, 3910-090-500, 3910-090-502, 3910-090-650, 3910-090-652, 3910-090-800, and 3910-090-802. The obturator is used to create an opening… |
| Product code | HRX |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 10, 2011 |
| 510(k) numbers | K944210 |
| 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