Device recall
Z-2635-2010: Enseal TRIO Product Code ETRIO335H, Lot Code: G4TC14, Exp. Date 2012/05
FDA device recall · Class II · Ethicon Endo-Surgery Inc
Key facts
| Recall number (Z-number) | Z-2635-2010 |
|---|---|
| Recall event | 56292 |
| Product | Enseal TRIO Product Code ETRIO335H, Lot Code: G4TC14, Exp. Date 2012/05 |
| Product code | NLM |
| Recalling firm | Ethicon Endo-Surgery Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 14, 2011 |
| 510(k) numbers | K070165, K070896, K072177 |
| FEI number | 1527736 |
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