Device recall
Z-3274-2011: Stryker SmartPump Extension Tubing (Pneumatic tourniquet). Sterile tubing…
FDA device recall · Class III · Stryker Instruments Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-3274-2011 |
|---|---|
| Recall event | 59791 |
| Product | Stryker SmartPump Extension Tubing (Pneumatic tourniquet). Sterile tubing extension 40" and 60", set, luer lock. Rx only. Stryker Instruments Div. of Stryker Corporation. Optional accessories used with the Stryker SmartPump Tourniquet System. The luer locks are intended to be connected to the… |
| Product code | KCY |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 12, 2011 |
| 510(k) numbers | K952038 |
| FEI number | 1811755 |
At a glance
- 1–9 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