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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Rover Mobile X-ray Systems Recalled Due to Generator Malfunction

Agency Publication Date: April 22, 2026
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Summary

Micro-X Ltd. is recalling 32 units of its Rover Mobile X-ray System, models MXU-RV35 and MXU-RV71, because the X-ray generator may malfunction. This defect can cause the X-ray system to become completely inoperable during use. No incidents or injuries have been reported at this time.

Risk

The X-ray generator may fail, which prevents the device from producing X-ray images, potentially delaying critical medical diagnosis or treatment for patients.

What You Should Do

  1. Identify if your device is affected by checking the model and serial numbers. The recall affects Model MXU-RV71 with serial numbers 334, 397, 399, 408, 423, 425, and 459, as well as Model MXU-RV35 with multiple serial numbers including 269, 223, 349, 348, and 351. See the Affected Products section below for the full list of affected codes.
  2. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  3. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding medical device recalls.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Rover Mobile X-ray System
Model / REF:
MXU-RV35
MXU-RV71
Serial Numbers:
334
397
399
408
423
425
459
269
223
349
348
351
363
388
384
391
359
416
419
428
429
430
431
435
434
436
413
437
438
460
461
462
UDI:
09357123000051
09357123000037

Refer to product traceability spreadsheet provided by manufacturer.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98644
Status: Active
Manufacturer: Micro-X Ltd.
Sold By: Micro-X Ltd.
Manufactured In: Australia
Units Affected: 32
Distributed To: Washington, New Jersey, California, Puerto Rico

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.