FDAJanuary 5, 2025device

VARIPULSE Bi-Directional Ablation Catheter REF D141201. The Field Catheter is indicated for use in catheter based cardiac electrophysiological mapping (stimulating and recording) and, when used for TRUPULSE Generator, for the treatment of drug refractory recurrent symptomatic paroxysmal atrial fi...

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

The hazard

Due to an observed trend of neurovascular events

What to do

FDA enforcement status: Ongoing

Brands named

biosense websterbiosense

UPCs

10846835025460

Recall history

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

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