Device recall
Z-1341-2023: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1341-2023 |
|---|---|
| Recall event | 91849 |
| Product | Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4,1BLA,1PRT QUICK Catalog number: 5921-034-135NS Indicated for use in surgical procedures that require the temporary occlusion of blood flow in a patient s extremities |
| Product code | KCY |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015967359 |
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