Stryker Ureteral Universal Kit, Model number 220-180-517, The ureteral kit is a ureteral transillumination device with r
FDA device recall Z-1867-2008 · posted 2008-09-16 · Terminated
Recall details
- Recalling firm
- Stryker Endoscopy
- Reason for recall
- Kit fibers may not illuminate along entire length, which may result in inadequate visibility of the urethral structures during surgery
- Action taken
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- FCS
- Quantity affected
- 1195 units
- Distribution
- Product was distributed nationwide and to Australia, Canada, Scandinavia, Italy and Switzerland
- Date initiated
- 2008-05-09
- Date posted
- 2008-09-16
- Date terminated
- 2010-12-21
- Location
- San Jose, CA
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