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CardioFocus Recalls

1 recall on record · March 19, 2025 to March 19, 2025 · Medical Devices

March 19, 2025Medical DevicesFDA

CardioFocus, Inc. recalls CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in

Hazard: Damage to the sterile barrier pouch of catheter, which could potentially compromise its sterility.

CardioFocus Recalls | RecallWatchUSA