Biosense Webster, Inc.: Medical Device Recalls in 2025

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Biosense Webster, Inc. in 2025. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

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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 fibrillation. The catheter provides location information when used with the CARTO 3 System.