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)