FDA recall record

MICRO-X Rover Mobile X-ray System, # MXU-RV35 recall — FDA Z-0664-2025

Shots were terminated by the mAs integrator; however, the 4 ms exposure time did not allow enough tolerance to achieve diagnostic exposures due to…

Class IIclassification
Z-0664-2025official record ID
Dec 18, 2024report date

Recall record at a glance

Official recordZ-0664-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMicro-X Ltd.
Report dateDec 18, 2024
Recall initiation dateMay 31, 2023
Quantity5
LocationTonsley, Australia

Official product description

MICRO-X Rover Mobile X-ray System, # MXU-RV35

Why the product was recalled

Shots were terminated by the mAs integrator; however, the 4 ms exposure time did not allow enough tolerance to achieve diagnostic exposures due to variations in hardware and how different timers are started.

Distribution information

Worldwide and US Nationwide Distribution: NJ, PR, CA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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