FDAJuly 13, 2021device

EV3 Pipeline Flex Embolization Device with Flex Shield Technology

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

Recall history

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

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