Z-2024-2019 Class II Terminated

Recalled by Siemens Medical Solutions USA, Inc — Malvern, PA

Recall Details

Product Type
Devices
Report Date
July 31, 2019
Initiation Date
June 12, 2019
Termination Date
September 18, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
39

Product Description

AXIOM Artis dFA, Model Number 7555373

Reason for Recall

A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.

Distribution Pattern

US Nationwide Distribution

Code Information

Serial Numbers: 50063 50059 50006 50064 50189 50044 50074 50101 51719 50062 50065 50087 50167 50039 50084 51706 51707 50048 50161 50093 50206 50057 50081 50133 50040 50016 50120 50191 51701 50027 51700 50139 50004 50010 50024 50142 50079 50132 50050