Device recall
Z-0147-2015: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open…
FDA device recall · Class II · CooperSurgical, Inc. D.B.A. Lone Star Medical Products
Key facts
| Recall number (Z-number) | Z-0147-2015 |
|---|---|
| Recall event | 69446 |
| Product | Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy. |
| Product code | DRC |
| Recalling firm | CooperSurgical, Inc. D.B.A. Lone Star Medical Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 23, 2015 |
| 510(k) numbers | K911462 |
| FEI number | 1627186 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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