FDAJuly 13, 2021device

Pipeline Flex Embolization Device

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

The hazard

Due to potential push wire fractures in the delivery system during use. The issue presents as a fracture in the spiral cut area of the Hypotube.

What to do

FDA enforcement status: Ongoing

Brands named

micro therapeuticsmicro

UPCs

008475360143430084753601437400847536014404008475360144350084753601446600847536014497008475360145270084753601455800847536014589008475360146190084753601464000847536014671

Recall history

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

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