Siemens recalls Mobilett Mira wireless (VA2:0) mobile x-ray systems due to no acoustic signal during x-ray activation. The system functions correctly but requires visual confirmation of x-ray release.
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.
Siemens is recalling Mobilett Mira wireless mobile x-ray systems because the buzzer isn't mounted correctly, so there's no sound when the x-ray activates. This means the operator must rely on the visual LED light to confirm the x-ray is happening, which could lead to missed exposures if not monitored properly.
The buzzer component is mounted incorrectly, so there is no acoustic signal when the x-ray activates. The system still works correctly for x-ray imaging, but the operator must use the visual LED light to confirm the x-ray release. If the operator misses the visual indicator, they might not realize an x-ray has been taken.
Healthcare professionals using Siemens Mobilett Mira wireless x-ray systems for medical imaging are most at risk. Patients and staff could be affected if the x-ray is not properly monitored due to the lack of sound.
Check for the model number 10273100 or UDI 04056869009117 on the system. The recall applies to Mobilett Mira wireless (VA20) mobile x-ray systems sold with these identifiers.
Ensure the exposure LED light is visible to confirm x-ray activation, as there is no acoustic signal.
The buzzer component is mounted incorrectly, so there is no acoustic signal during x-ray activation. The system functions correctly but requires visual confirmation of x-ray release.
Yes, the system is fully functional for x-ray imaging, but the operator must use the visual LED light to confirm x-ray release to avoid missed exposures.
Model number 10273100 and UDI 04056869009117 are affected.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0223-2024 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0223-2024 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
