Use caution Medical device recall · FDA · Published October 5, 2023

Siemens Mobilett Mira Wireless X-Ray System Recall: No Acoustic Signal During X-Ray

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0223-2024Medical device Siemens ›

Use caution until it’s fixed

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.

Take action

Contact the company

Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd · Malvern, PA 19355-1418

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/57150-siemens-mobilett-mira-wireless-x-ray-system-recall-no-acoustic.

Source Summary by GovInfoNow · govinfonow.com/recall/57150-siemens-mobilett-mira-wireless-x-ray-system-recall-no-acoustic · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0223-2024

Cite this page

“Siemens Mobilett Mira Wireless X-Ray System Recall: No Acoustic Signal During X-Ray.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57150-siemens-mobilett-mira-wireless-x-ray-system-recall-no-acoustic. Based on FDA recall #Z-0223-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0223-2024%22&limit=1).

The FDA announced on 2023-10-05 that Siemens Medical Solutions USA, Inc. is recalling Mobilett Mira wireless (VA20) mobile x-ray systems due to a missing acoustic signal during activation. Four units distributed nationwide are affected by this Class II recall.

How to tell if you have it

Brand: Siemens
Product: Mobilett Mira wireless (VA20) mobile x-ray system
Model Number: 10273100
UDI: 04056869009117
Serial Numbers: 1511, 2168, 2525, 2633

The hazard

According to the FDA, the incorrect mounting of the buzzer component results in no acoustic signal during x-ray activation. The system remains fully functional, and operators can monitor x-ray release via a visual indicator or view the clinical image on the monitor after exposure.

Context

GovInfoNow's records show Siemens Medical Solutions USA, Inc. has 182 other recalls on record since 2017-06-06. Recent brand recalls include a 2026-06-08 ARTIS icono Ceiling Monitor recall for loose screws and a 2026-05-20 ARTIS icono ceiling recall regarding loss of movement after extreme height adjustments. Other recent recalls of similar products include the 2026-03-27 Micro-X Rover Mobile X-ray System Recall, the 2026-07-24 Spectral Instruments Ami HTX Recall, and the 2026-03-03 Philips Azurion 5 M12 X-ray System May Not Start Properly - Recall.

How to tell if you have this one

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.

Brand
Siemens
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Visual Indicator
Ensure the exposure LED light is visible to confirm x-ray activation, as there is no acoustic signal.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “US Nationwide - Worldwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 48 days after the firm started it.

Oct 5, 2023Firm started the recall
Nov 14, 2023FDA classified it Class II
Nov 22, 2023Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest medical device recalls

Keep exploring

More Siemens recalls

Link to this recall

<a href="https://govinfonow.com/recall/57150-siemens-mobilett-mira-wireless-x-ray-system-recall-no-acoustic">Siemens Mobilett Mira Wireless X-Ray System Recall: No Acoustic Signal During X-Ray (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-0223-2024 (October 5, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0223-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.