Device recall
Z-0908-2009: Expressaire, Disposable Tourniquet Cuff 34", 2 line (18), sterile, Manufactured…
FDA device recall · Class II · Virtus, Inc.
Key facts
| Recall number (Z-number) | Z-0908-2009 |
|---|---|
| Recall event | 50750 |
| Product | Expressaire, Disposable Tourniquet Cuff 34", 2 line (18), sterile, Manufactured for Sammons Preston, A Patterson Medical Company, Cedarburg, WI.; Cuff type A70107011. Each cuff is marked ExpressAire by Sammons Preston and A70107011. The tourniquet cuff is placed on a patient's thigh during an… |
| Product code | KCY |
| Recalling firm | Virtus, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2010 |
| FEI number | 1824206 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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