Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Micro-X Rover Mobile X-ray Systems Recalled for Capacitor Malfunction

Agency Publication Date: November 27, 2024
Share:
Sign in to monitor this recall

Summary

Micro-X Ltd. is recalling six units of the Rover Mobile X-ray System (model MXU-RV35) due to a potential capacitor malfunction. This malfunction can cause the device to overheat, start up unexpectedly, or exhibit unpredictable behavior if specific storage and operating conditions regarding temperature and humidity are not met. While no injuries or incidents have been reported, the manufacturer has issued this voluntary recall to mitigate safety risks associated with electrical failure.

Risk

The capacitors in the x-ray system can fail if the device is exposed to environmental conditions outside of specific limits, such as high humidity or temperature gradients. This failure can lead to the system overheating or starting up without user intervention, potentially causing device damage or interfering with medical procedures.

What You Should Do

  1. This recall involves Micro-X Rover Mobile X-ray Systems (model MXU-RV35) with serial numbers 348, 349, 361, 351, 365, and 391.
  2. Check the device label on your mobile x-ray unit to confirm the model number and serial number. The affected units have a Unique Device Identifier (UDI-DI) of 9357123000037.
  3. Stop using the recalled device. Contact Micro-X Ltd. or your authorized medical device distributor to arrange for a return, replacement, or correction of the unit.
  4. Ensure any units still in use are strictly following storage and operation requirements: temperature between 50°F and 86°F, relative humidity between 30% and 60%, and altitude between -102 feet and 12,000 feet.
  5. Call the FDA at 1-888-463-6332 for more information regarding this medical device recall.

Your Remedy Options

📋Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: MICRO-X Rover Mobile X-ray System
Model / REF:
MXU-RV35
Serial Numbers:
348
349
361
351
365
391
UDI:
9357123000037

Recall number Z-0580-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95624
Status: Active
Manufacturer: Micro-X Ltd.
Sold By: Authorized medical device distributors
Manufactured In: Australia
Units Affected: 6
Distributed To: Texas, Puerto Rico, Maryland, California

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 · 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.