Device recall
Z-1866-2008: Stryker Ureteral Kit, Model number 220-180-516, The ureteral kit is a ureteral…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-1866-2008 |
|---|---|
| Recall event | 48218 |
| Product | Stryker Ureteral Kit, Model number 220-180-516, The ureteral kit is a ureteral transillumination device with reusable illumination source and a fiberoptic light ureteral catheter kit which is provided sterile for single use disposable application. The device is intended to be used to transilluminate… |
| Product code | FCS |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2010 |
| 510(k) numbers | K982542 |
| FEI number | 2936485 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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