Device recall
Z-0013-2012: Natura Durahesive ConvaTec Moldable Technology Post-Operative /Surgical System…
FDA device recall · Class III · Convatec Inc.
Key facts
| Recall number (Z-number) | Z-0013-2012 |
|---|---|
| Recall event | 59952 |
| Product | Natura Durahesive ConvaTec Moldable Technology Post-Operative /Surgical System (57 mm) Required for application to a patient immediately after ostomy surgery. |
| Product code | EXB |
| Recalling firm | Convatec Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 11, 2012 |
| 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