Device recall
Z-1673-2008: Tourniquet Cuff Single Port Single Bladder - Reprocessed Sterile device…
FDA device recall · Class II · Ascent Healthcare Solutions, Inc.
Key facts
| Recall number (Z-number) | Z-1673-2008 |
|---|---|
| Recall event | 47343 |
| Product | Tourniquet Cuff Single Port Single Bladder - Reprocessed Sterile device -- Pneumatic tourniquet. |
| Product code | KCY |
| Recalling firm | Ascent Healthcare Solutions, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2012 |
| FEI number | 1000132435 |
At a glance
- None Linked 510(k)s
- 10–99 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