Cook Inc. recalls Kwart Retro-Inject Ureteral Stent Set, Global Product No. G
Recalled Product
Kwart Retro-Inject Ureteral Stent Set, Global Product No. G15016 G14836 G14885 G14887 G17151
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: 8011027 8183322 8037660 8030233 8018054 7994816
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