Device recall
Z-0073-2011: ActiveLife One-Piece Drainable Pouch with Stomahesive Skin Barrier; 1 1/4 in…
FDA device recall · Class III · Convatec Inc.
Key facts
| Recall number (Z-number) | Z-0073-2011 |
|---|---|
| Recall event | 56789 |
| Product | ActiveLife One-Piece Drainable Pouch with Stomahesive Skin Barrier; 1 1/4 in., 32mm; Made in Dominican Republic; ConvaTec. Colostomy pouch |
| Product code | EZQ |
| Recalling firm | Convatec Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 19, 2010 |
| FEI number | 3011987967 |
At a glance
- None 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