Product Safety Recalls

Product Recall Tracker

Siemens Medical Solutions USA, Inc Recall 88962

Description: Artis Q floor with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848280

Siemens Medical Solutions USA, Inc Recall 88962 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0300-2022
Event ID88962
Event DescriptionArtis Q floor with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848280
Product TypeDevices
DistributionUS Nationwide Distribution
Quantity8 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 104007 104016 104005 104027 104012 104025 104013 132500 Expanded Recall 11/15/21: 104029 104020
Center Classification Date20211124
Recall Initiation Date20211020
Recalling FirmSiemens Medical Solutions USA, Inc
Initial Notification Letter
Similar To

© 2021 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.