Stryker Endoscopy Stryker Ureteral Universal Kit, Model number 220-180-517, 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 the ureter during laparoscopic and open surgical procedures of the lower abdomen or pelvic areas to help the surgeon identify the ureter. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Ureteral Universal Kit, Model number 220-180-517, 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 the ureter during laparoscopic and open surgical procedures of the lower abdomen or pelvic areas to help the surgeon identify the ureter.
Brand
Stryker Endoscopy
Lot Codes / Batch Numbers
Lot numbers 4025, 4169, 4362, 4647, 4711, 5196, and 5461
Products Sold
Lot numbers 4025, 4169, 4362, 4647, 4711, 5196, and 5461
Stryker Endoscopy is recalling Stryker Ureteral Universal Kit, Model number 220-180-517, The ureteral kit is a ureteral transillumi due to Kit fibers may not illuminate along entire length, which may result in inadequate visibility of the urethral structures during surgery. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Kit fibers may not illuminate along entire length, which may result in inadequate visibility of the urethral structures during surgery
Recommended Action
Per FDA guidance
Sales representatives were notified via telephone, and recall product advisory notices will be sent to all consignees on 05/09/2009. Contact a Regulatory Affairs representative at 408-754-2161 or 408-754-2000 should you have any questions.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026