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Recall Observatory FDA recall evidence

Device product

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

Z-0300-2022

October 20, 2021

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 88962
Status
Terminated
Classification
Class II
Quantity
8 units
Official record key
device-enforcement:Z-0300-2022

Official wording

Reason: 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

Code information: Serial Numbers: Serial 104007 104016 104005 104027 104012 104025 104013 132500 Expanded Recall 11/15/21: 104029 104020

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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