FDAOctober 5, 2023device

Mobilett Mira wireless (VA20) mobile x-ray system(s)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Otherwise, the system is fully functional, and x ray is applied correctly. By means of the additional visual indicator (exposure LED light) the operator can monitor the x ray release. Also, after a successful x ray exposure, the clinical image is displayed on the monitor.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

04056869009117

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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