Device recall
Z-2794-2011: Stryker 4.0 mm. Angled Aggressive 12 Degree Blade, Precision Cutters, Stryker…
FDA device recall · Class II · Stryker Instruments Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2794-2011 |
|---|---|
| Recall event | 59057 |
| Product | Stryker 4.0 mm. Angled Aggressive 12 Degree Blade, Precision Cutters, Stryker Instruments, Kalamazoo, MI 49001 USA, (269) 323-7700 (800) 253-3210, Sterile, Single Use, Rx ONLY For Functional Endoscopic Sinus Surgery for the incision of soft and osseous tissue in the sinus cavities, open plastic, and… |
| Product code | GFA |
| Recalling firm | Stryker Instruments Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 3, 2011 |
| FEI number | 1811755 |
At a glance
- None 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