FDA Recall Terminated

Artis zee floor MN, Model Number 10094142

Recall: Z-2032-2019 · Initiated June 12, 2019

Recall

Recall Number
Z-2032-2019
Event Number
83203
Firm
Siemens Medical Solutions USA, Inc
FEI Number
2240869
Product Code
OWB
Status
Terminated
Root Cause
Component design/selection
Initiated
June 12, 2019
Terminated
September 18, 2020
Address
40 Liberty Blvd, Malvern, PA, 19355-1418

Description

Artis zee floor MN, Model Number 10094142

Reason

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.

Action

Urgent Medical Device Correction notification letters dated 6/12/19 were sent to customers. In the event the issue occurs, the system cannot be operated normally as X-ray will not possible. Planned procedures may have to be terminated and performed on an alternative X-ray system. Siemens advises that an alternative system is available to continue treatment in case of occurrence. Siemens is implementing a corrective action to all potentially affected users of the Artis Zee and AXIOM Artis systems with generator A100 via Update Instruction AX038/18/S. The Siemens Service organization will modify the affected supply circuit and revise the wiring. This modification will bring the voltage back to the center of the tolerance range. Our service organization will contact you shortly to arrange a date to perform this corrective action. Please feel free to contact our service organization for an earlier appointment at 1-800-888-7436. Following the correction, the cause is eliminated and any recurrence of this potential fault is prevented.

Distribution

US Nationwide Distribution

Quantity

23