FDAFDA · Food and drugs·Recall number Z-0300-2025
Boston Scientific POLARx FIT BALLOON CATHETER ST US, Material Number M004CRBS2060
Published November 20, 2024 · Recall initiated: October 10, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Boston Scientific Corporation
- Distributor
- Worldwide
- Lot
- GTIN 08714729992622
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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