Device recall
Z-0465-2014: Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use…
FDA device recall · Class II · Karl Storz Endoscopy America Inc
Key facts
| Recall number (Z-number) | Z-0465-2014 |
|---|---|
| Recall event | 66823 |
| Product | Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue. |
| Product code | GCJ |
| Recalling firm | Karl Storz Endoscopy America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2014 |
| 510(k) numbers | K934937 |
| FEI number | 2020550 |
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