FDAFebruary 14, 2020device

ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

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

The hazard

Embolization device delivery system may fracture at the distal section during device implantation. A weakened bond may result in unintended separation, where the distal portion of the device delivery system remains in the patient. If a Pipeline Flex embolization device has already been implanted successfully, there is no increased risk to patients due to this issue.

What to do

FDA enforcement status: Terminated

Brands named

micro therapeutics inc dba ev3 neurovascularmicromicro therapeutics

Recall history

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

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