AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553680
FDA Recall #Z-1028-2025 — Class II — December 20, 2024
Product Description
AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553680
Reason for Recall
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.
Recalling Firm
Boston Scientific Corporation — Marlborough, MA
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
31 units
Distribution
Nationwide including Puerto Rico Foreign: To be provided
Code Information
GTIN: 00191506008086 Lot Numbers: 33457806, 33512838, 34035520
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated