FDA Enforcement
Class II
Ongoing
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553520
Recall: Z-1032-2025
·
Reported February 5, 2025
Enforcement
- Recall Number
- Z-1032-2025
- Event ID
- 96049
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Boston Scientific Corporation
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- February 5, 2025
- Initiation Date
- December 20, 2024
- Classification Date
- January 30, 2025
- Address
- 100 Boston Scientific Way, Marlborough, MA, 01752-1234, United States
Description
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553520
Reason
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
Code Info
GTIN: 08714729904540 Lot Numbers: 33336402, 33336404, 33336405, 33336411, 33392916, 33392917, 33393302, 33411607, 33437479, 33548501, 33577903, 33704371, 33712822, 33986537, 34017087, 34017088, 34017089, 34028458, 34065579, 34065660, 34083271, 34083272
Distribution
Nationwide including Puerto Rico Foreign: To be provided
Quantity
263 units (OUS)