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Siemens Medical Solutions USA, Inc recalls Artis Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and intervent
Recalled December 1, 2021 · FDA recall Z-0301-2022 · Siemens Medical Solutions USA
Hazard
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 · FDA Class II
Units
67 units
Sold at
US Nationwide Distribution
Description
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
Product
Artis Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848281
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →