FDAJune 10, 2025device

Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM 55DEG Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, including the left atrium via transseptal perforatio...

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

The hazard

Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

0068544700539100685447005407

Recall history

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

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