Device recall
Z-2751-2011: Brand REMOVE Universal Adhesive Remover Wipe - Pouch Label and 50 count box…
FDA device recall · Class II · Smith & Nephew Inc.
Key facts
| Recall number (Z-number) | Z-2751-2011 |
|---|---|
| Recall event | 58525 |
| Product | Brand REMOVE Universal Adhesive Remover Wipe - Pouch Label and 50 count box Label: ***smith&nephew***#403100*** REMOVE Universal Adhesive Remover Wipes Gently removes tapes and adhesives Reduces risk of irritation and skin stripping Contains Aloe***1 wipe and 50 wipes*** For external use only. Avoid… |
| Product code | KOX |
| Recalling firm | Smith & Nephew Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2011 |
| FEI number | 3006760724 |
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