FDA Recall Terminated

ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model Number 10849000

Recall: Z-3190-2018 · Initiated July 29, 2018

Recall

Recall Number
Z-3190-2018
Event Number
80905
Firm
Siemens Medical Solutions USA, Inc
FEI Number
2240869
Product Code
OWB
Status
Terminated
Root Cause
Device Design
Initiated
July 29, 2018
Terminated
May 17, 2019
Address
40 Liberty Blvd, Malvern, PA, 19355-1418

Description

ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model Number 10849000

Reason

Temperature of the detector may fall out of its designed working range (cool down) due to incorrectly configured temperature control unit. This unintentional system behavior may occur while the unit is powered down for long periods (e.g. at night).

Action

Urgent Medical Device Correction notification letters dated 7/27/18 were distributed to customers. The letters informed the customers of the following planned actions: Our service organization will contact you shortly to arrange a date to perform this corrective action with Update Instruction AX001/18/S. Please feel free to contact our service organization for an earlier appointment at 1-800-888-7436. Following the corrective action, the cause is eliminated and a recurrence of the fault is prevented. Additionally, Siemens is developing a solution to restore the system back to the original settings. This solution will be distributed to all affected customers upon completion.

Distribution

US nationwide distribution.

Quantity

429 total