Device recall
Z-1055-04: LIGACLIP ERCA Endoscopic Rotating Multiple Clip Applier (Product Code: ER320)…
FDA device recall · Class II · Ethicon Endo-Surgery
Key facts
| Recall number (Z-number) | Z-1055-04 |
|---|---|
| Recall event | 29269 |
| Product | LIGACLIP ERCA Endoscopic Rotating Multiple Clip Applier (Product Code: ER320) and assorted Flex Trays(Convenience Kits), containing ER320, LIGACLIP ERCA Endoscopic Rotating Multiple Clip Appliers. |
| Product code | GDO |
| Recalling firm | Ethicon Endo-Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2008 |
| 510(k) numbers | K864102 |
| FEI number | 1527736 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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