Device recall
Z-1530-2013: ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister pack…
FDA device recall · Class II · Ethicon Endo-Surgery Inc
Key facts
| Recall number (Z-number) | Z-1530-2013 |
|---|---|
| Recall event | 65330 |
| Product | ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister pack with Tyvek lid. The ECHELON and ECHELON FLEX families of Endoscopic Linear Cutters (articulating and straight) are sterile, single patient use instruments that simultaneously cut and staple tissue. There are six staggered… |
| Product code | GDW |
| Recalling firm | Ethicon Endo-Surgery Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 11, 2014 |
| 510(k) numbers | K112056 |
| FEI number | 1527736 |
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