FDAJune 10, 2025device

VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device approved and commercialized in Japan only.

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

00685447006121

Recall history

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

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VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device approved and commercialized in Japan only. — Recall Details · AllClear