Device recall
Z-0873-06: Sterile packaged wound dressing with white and green inner pouch and outer…
FDA device recall · Class II · Kinetic Concepts, Inc
Key facts
| Recall number (Z-number) | Z-0873-06 |
|---|---|
| Recall event | 35089 |
| Product | Sterile packaged wound dressing with white and green inner pouch and outer carton labels, labeled in part:''***V.A.C.*** ABDOMINAL DRESSING WITH NON ADHERENT LAYER***Re-Order No. M6275080/5***Manufactured for Corporate Headquarters: KCI USA, Inc., 8023 Vantage Dr., San Antonio, TX 78230 USA***''. |
| Product code | FTL |
| Recalling firm | Kinetic Concepts, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 22, 2006 |
| 510(k) numbers | K022011 |
| FEI number | 1625774 |
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