FDADecember 1, 2020device

Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm (OUS) UPN: M00553560 - Product Usage: The stent is intended for implantation up to 60 days and should be removed upon confirmation of pseudocyst or walled-off necrosis resolution.

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

The hazard

The rotating luer fitting at the distal end of the delivery system handle may become detached from the nose of the delivery during device preparation, stent delivery or use, resulting in delay or procedure or risk of peritonitis developing from leakage of enteric, pseudocyst, or biliary contents into the peritoneal cavity

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

UPCs

08714729951100

Recall history

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

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