FDA Device Recalls

Recalls /

#190129

Product

Artis zee floor with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10094135

FDA product code
OWBInterventional Fluoroscopic X-Ray System
Device class
Class 2
Medical specialty
Radiology
510(k) numbers
K181407
Affected lot / code info
Serial Numbers: 124703 139012 139023

Why it was recalled

If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result in a short delay in procedure

Root cause (FDA determination)

Software design

Action the firm took

Siemens Medical Solutions USA, Inc. initiated a Customer Safety Advisory Notice dated 10/202/1 to customers via AX070/21/S, Siemens will update the system software via Update Instruction AX069/21/S. Letter states reason for recall, health risk and action to take: To avoid the problem, it is recommended to position the SID first and then release x-ray. Siemens will correct the software error (software VD12) via Update Instruction AX069/21/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. We do not consider it necessary to re-examine any patients in relation to the issues described above. Please review, understand, and confirm acknowledgement of the information and instructions outlined in this Urgent Safety Advisory Notice. By signing this document, you are acknowledging that you have read and understand the content therein

Recalling firm

Firm
Siemens Medical Solutions USA, Inc
Address
40 Liberty Blvd, Malvern, Pennsylvania 19355-1418

Distribution

Distribution pattern
US Nationwide Distribution

Timeline

Recall initiated
2021-10-20
Terminated
2024-06-18
Status

Source: openFDA Device Recall endpoint. Recall record ID #190129. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.