Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71, MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring medical diagnostic images outside a standard X-ray room. It is designed specifically for Digital Radiography (DR) with vendor-supported detectors. The Rover is designed to perform radiographic X-ray examinations for disease/injury detection, diagnosis, medical and surgical treatment planning, and therapy monitoring, where patient condition contraindicates transport to a fixed X-ray unit The Rover can be used on pediatric and adult patients, in all patient treatment areas Component: N/A
FDA Recall Z-1669-2025 · Posted 2025-04-24
Recalling FirmMicro-X Ltd.
Recall StatusOpen, Classified
Product CodeIZL
Date Initiated2025-04-04
Product Quantity13 units
Reason for Recall
Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
Firm Action
On April 4, 2025, Micro-X Ltd. issued a "Urgent Medical Device Correction" Notification to via E-Mail affected consignees. Micro-X ask consignees to take the following actions:
" Inspect your stock immediately and quarantine affected stock on hand to prevent further use.
" Circulate this notice to all users of this device so they are aware of the issue.
" If the product has been further distributed to other facilities, please ensure this notice is immediately shared with them.
" Please retain this letter with your system(s) documentation.
" Please complete and return the attached response form to the Micro-X LTD in Australia: [email protected] and copy [email protected] to reconcile this process no later than 30 days from receipt. Completing this form confirms receipt of this notice, understanding of the issue, and the necessary actions to be taken.
Root Cause
Device Design
Distribution Pattern
US: NJ, WA, Puerto Rico OUS: None
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.