Device recall
Z-0736-05: FlexTrayTM Endopath GYN Tray, Kit code KD005.
FDA device recall · Class II · Ethicon Endo-Surgery
Key facts
| Recall number (Z-number) | Z-0736-05 |
|---|---|
| Recall event | 30727 |
| Product | FlexTrayTM Endopath GYN Tray, Kit code KD005. |
| Product code | MDM |
| Recalling firm | Ethicon Endo-Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 30, 2012 |
| FEI number | 1527736 |
At a glance
- None Linked 510(k)s
- 10–99 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