PlainRecalls
FDA Devices Critical Class I Ongoing

Boston Scientific POLARx FIT BALLOON CATHETER LT US, Material Number M004CRBS2160

Reported: November 20, 2024 Initiated: October 10, 2024 #Z-0302-2025

Product Description

Boston Scientific POLARx FIT BALLOON CATHETER LT US, Material Number M004CRBS2160

Reason for Recall

Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.

Details

Units Affected
368 units
Distribution
Worldwide
Location
Saint Paul, MN

Frequently Asked Questions

What product was recalled?
Boston Scientific POLARx FIT BALLOON CATHETER LT US, Material Number M004CRBS2160. Recalled by Boston Scientific Corporation. Units affected: 368 units.
Why was this product recalled?
Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 20, 2024. Severity: Critical. Recall number: Z-0302-2025.