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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Rover Mobile X-ray Systems Recalled Due to Internal Generator Failure

Agency Publication Date: April 24, 2025
Share:
Sign in to monitor this recall

Summary

Micro-X Ltd. has recalled 18 units of its Rover Mobile X-ray System (models MXU-RV71 and MXU-RV35) because an internal fastening mechanism within the device's generator can fail. This failure involves the mechanical assembly inside the self-contained X-ray unit. No injuries or incidents have been reported to date. These mobile systems are used in clinical settings and medical facilities to perform X-ray examinations outside of standard imaging rooms.

Risk

If the internal fastening mechanism within the X-ray generator fails, the mobile imaging system may malfunction or cease to operate during medical diagnostic procedures. This failure could lead to inaccurate medical images or delays in critical detection, diagnosis, or treatment planning for patients.

What You Should Do

  1. The recalled products are Rover Mobile X-ray Systems (Models MXU-RV71 and MXU-RV35) manufactured by Micro-X Ltd. Check the serial number on the device identification label. See the Affected Products section below for the full list of affected codes.
  2. Stop using the recalled mobile X-ray devices immediately.
  3. Contact Micro-X Ltd. or your authorized distributor to arrange for a return, replacement, or professional correction of the generator failure.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding this safety recall.

Your Remedy Options

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

Affected Products

Product: Rover Mobile X-ray System
Model / REF:
MXU-RV71
MXU-RV35
Serial Numbers:
352
334
389
383
384
382
386
385
387
388
364
390
395
UDI:
09357123000051

Recall #: Z-1669-2025; Quantity: 13 units.

Product: Rover Mobile X-ray System
Model / REF:
MXU-RV35
Serial Numbers:
349
348
350
351
361
UDI:
09357123000037

Recall #: Z-1670-2025; Quantity: 5 units.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96638
Status: Active
Manufacturer: Micro-X Ltd.
Sold By: Authorized distributors; Medical facilities
Manufactured In: Australia
Units Affected: 2 products (13 units; 5 units)
Distributed To: New Jersey, Washington, 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.