FDAMarch 21, 2024device

Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 (5PK), REF H74908526032; cardiac catheter

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

The hazard

An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

08714729187707

Recall history

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

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