Product Safety Recalls

Product Recall Tracker

Siemens Medical Solutions USA, Inc Recall 88962

Description: Artis Q.zen ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848354

Siemens Medical Solutions USA, Inc Recall 88962 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0304-2022
Event ID88962
Event DescriptionArtis Q.zen ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848354
Product TypeDevices
DistributionUS Nationwide Distribution
Quantity15 units
Recall ReasonIf 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
Device Classification20211201
Device Code InfoSerial Numbers: Serial 111502 111503 111510 111507 111512 111508 111133 111504 111506 111513 111500 111501 111505 111514
Center Classification Date20211124
Recall Initiation Date20211020
Recalling FirmSiemens Medical Solutions USA, Inc
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.