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FDAJanuary 4, 2019device

C-Flex Double Pigtail Ureteral Stent Set, Global Product No. G14364 G14365 G14367

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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