AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740
FDA Recall #Z-1030-2025 — Class II — December 20, 2024
Product Description
AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740
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
12 units
Distribution
Nationwide including Puerto Rico Foreign: To be provided
Code Information
GTIN: 08714729904625 Lot Numbers: 34477280
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated