FDA Recall Terminated

ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 - Product Usage: is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.

Recall: Z-2108-2020 · Initiated April 22, 2020

Recall

Recall Number
Z-2108-2020
Event Number
85608
Firm
Siemens Medical Solutions USA, Inc
FEI Number
2240869
Product Code
OWB
Status
Terminated
Root Cause
Software design
Initiated
April 22, 2020
Terminated
October 9, 2020
Address
40 Liberty Blvd, Malvern, PA, 19355

Description

ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 - Product Usage: is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.

Reason

If the C-arm leaves its intended travel path due to a fault within the drivetrain, movements may be impacted or impossible and the area of interest cannot be reached. In the event the C-arms movements are not possible, the system can only be returned to normal operation with the support of a field service engineer

Action

Siemens issued Urgent Medical Device Correction dated 4/22/20 via AX074/19/S. Letter states reason for recall, health risk and action to take: Planned procedures may have to be terminated and performed on an alternative X-ray system. Please follow the standard emergency procedures you have in place in the event of system failures. It is recommended to consider reinforcing these emergency procedures until the update has been completed. Siemens will correct the error with a software patch in which the system will recognize a deviation of the intended travel path and unit movements are stopped immediately, similar to the activation of a proximity switch. The correction will be initiated via Update Instruction AX073/19/S. 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

105 systems