FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401
FDA Recall Z-2278-2025 · Posted 2025-08-08
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Recalling FirmBoston Scientific Corporation
Recall StatusOpen, Classified
Product CodeQZI
Date Initiated2025-06-25
Product Quantity445 units
Reason for Recall
The potentially impacted units were manufactured using specific equipment that may have caused cracks in the electrode bands on the catheter's distal end.
Firm Action
An Urgent Medical Device Removal - Immediate Action Required notification letter dated June 2025 was sent to customers.
Actions
1. Do NOT use affected product (Attachment 1), remove affected devices from your facility s inventory, segregate the units in a secure place until they can be returned to Boston Scientific.
2. Immediately post this information in a visible location near the affected products to ensure this information is readily accessible to all handlers and users of the device.
3. Forward this notice to any healthcare professional from your organization for awareness and to any organization where affected devices have been transferred.
4. Complete and return the enclosed Reply Verification Tracking Form per the enclosed instructions on page five.
5. Return affected product.
Email: [email protected]
Reach out to your local Boston Scientific representative with any questions.
Root Cause
Nonconforming Material/Component
Distribution Pattern
US Nationwide.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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