FDAFebruary 12, 2024device

Boston Scientific POLARSHEATH Steerable Sheath 12F, REF M004CRBS3050

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

The hazard

Boston Scientific has identified a tooling error in manufacturing which may have caused delamination of the inner lumen of the sheath shaft in a subset of POLARSHEATH devices. This could result in the embolization of a fragment during use (such as flushing of the sheath or introduction of the dilator or ablation catheter).

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

08714729992684

Recall history

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

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