Product Wiki · Recalls · U.S. FDA — Device Enforcement

Boston Scientific POLARx BALLOON CATHETER LT 28MM OUS, Material Number M004CRBS2100 — recall Z-0298-2025

U.S. FDA — Device Enforcement · United States · 2024-10-10 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0298-2025
Date of alert
2024-10-10
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Boston Scientific Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08714729992660
Reported risk: Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.