FDADecember 20, 2024device

AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553680

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

The hazard

Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

00191506008086

Recall history

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

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