FDAJune 25, 2025device

FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401

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

The hazard

The potentially impacted units were manufactured using specific equipment that may have caused cracks in the electrode bands on the catheter's distal end.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

00191506043148

Recall history

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

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