Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
FDA Recall Z-1918-2026 · Posted 2026-04-22
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Recalling FirmMicro-X Ltd.
Recall StatusOpen, Classified
Product CodeIZL
Date Initiated2026-03-27
Product Quantity32 units
Reason for Recall
X-Ray generator may malfunction resulting in the X-Ray being inoperable.
Firm Action
On March 27, 2026, Micro-X issued a Urgent: Medical Device Correction Notification, via E-Mail. Micro-X ask consignees to take the following actions:
" Contact your local service representative to arrange replacement of the PCBA with the updated version at the next scheduled visit or Preventative Maintenance. In the interim, customers may continue to use the device.
" To minimize the likelihood of system failure, the batteries should not be permitted to fully discharge. Any system errors or abnormal behaviours must be reported to your authorised service provider without delay.
" If the product has been further distributed to other facilities, please ensure this notice is immediately shared with them.
" Please complete and email the Customer Response Form in Appendix 1 to the Micro-X LTD in Australia: [email protected] and copy [email protected] Completing this form confirms receipt of this notice, understanding of the issue, and the necessary actions to be taken.
Root Cause
Component design/selection
Distribution Pattern
US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto Rico.
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.
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