Cook Inc. recalls Bander Ureteral Diversion Open-End Stent Set, Global Product
Recalled Product
Bander Ureteral Diversion Open-End Stent Set, Global Product No. G14822 G14823
Hazard / Issue
The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: 8011030 8033568 8063430 8063431 8150491 8417631 8417632 8587162 8587163 8590532 8590533 7990830 8003084 8033571 8063428 8590520 8590522 8629475 NS8629473
View official government recall
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