FDASeptember 7, 2022device

THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrophysiological mapping (stimulation and recording) and, in conjunction with an RF generator, for cardiac ablation.

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

The hazard

Manufacturing error resulted in potential contamination of Bi-Directional navigation catheter irrigation path with cellulose fibers that can cause 1) Failure of initial flushing inspection, 2) Insufficient irrigation causing catheter tip temperature increase, limiting the ability to deliver ablation, or 3) particles flushed through the catheter irrigation may have thrombogenic/toxic effect.

What to do

FDA enforcement status: Ongoing

Brands named

johnson johnson surgical visionjohnsonjohnson johnson

UPCs

10846835010183

Recall history

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

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THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrophysiological mapping (stimulation and recording) and, in conjunction with an RF generator, for cardiac ablation. — Recall Details · AllClear