Device recall
Z-1532-06: ActiveLife One-Piece Pre-Cut Closed End (ostomy) Pouch with skin barrier and…
FDA device recall · Class III · ConvaTec
Key facts
| Recall number (Z-number) | Z-1532-06 |
|---|---|
| Recall event | 36268 |
| Product | ActiveLife One-Piece Pre-Cut Closed End (ostomy) Pouch with skin barrier and filter 45mm (box of 60) 1 3/4 in. 45 mm |
| Product code | LNO |
| Recalling firm | ConvaTec |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 10, 2007 |
| 510(k) numbers | K840568 |
| FEI number | 3011987967 |
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