FDAClass INovember 20, 2024

Boston Scientific POLARx FIT BALLOON CATHETER ST OUS recall

Boston Scientific POLARx FIT BALLOON CATHETER ST OUS, Material Number M004CRBS2010

Why was Boston Scientific POLARx FIT BALLOON CATHETER ST OUS recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

GTIN 08714729992578

Product
Boston Scientific POLARx FIT BALLOON CATHETER ST OUS, Material Number M004CRBS2010
Recalling firm
Boston Scientific Corporation
Quantity
5913 units
Distribution
Worldwide
Recall date
November 20, 2024
Classification
Class I
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls