Device recall
Z-1067-2014: Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound…
FDA device recall · Class II · Smith & Nephew Inc.
Key facts
| Recall number (Z-number) | Z-1067-2014 |
|---|---|
| Recall event | 66893 |
| Product | Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System |
| Product code | OMP |
| Recalling firm | Smith & Nephew Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2014 |
| FEI number | 3006760724 |
At a glance
- None 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