Device recall
Z-0016-04: Acticoat* Moisture Control Dressing, Product Code 20211, Distributed by Smith &…
FDA device recall · Class III · Smith And Nephew, Inc. Wound Management Division
Key facts
| Recall number (Z-number) | Z-0016-04 |
|---|---|
| Recall event | 26318 |
| Product | Acticoat* Moisture Control Dressing, Product Code 20211, Distributed by Smith & Nephew, Inc., Wound Management Division, 11775 Starkey Road, Largo, FL 33773 |
| Recalling firm | Smith And Nephew, Inc. Wound Management Division |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 11, 2012 |
| 510(k) numbers | K000051 |
| FEI number | 3006760724 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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