AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750
FDA Recall #Z-1031-2025 — Class II — December 20, 2024
Product Description
AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750
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
38 units
Distribution
Nationwide including Puerto Rico Foreign: To be provided
Code Information
GTIN: 08714729904632 Lot Numbers: 33740402, 33785754, 34037422
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated