FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401
Recall
- Recall Number
- Z-2278-2025
- Event Number
- 97207
- Firm
- Boston Scientific Corporation
- FEI Number
- 2124215
- Product Code
- QZI
- Status
- Open, Classified
- Root Cause
- Nonconforming Material/Component
- Initiated
- June 25, 2025
- Posted
- August 8, 2025
- Address
- 4100 Hamline Ave N, Saint Paul, MN, 55112-5700
Description
FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401
The potentially impacted units were manufactured using specific equipment that may have caused cracks in the electrode bands on the catheter's distal end.
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.
US Nationwide.
445 units