Micro-X recalls specific model Rover Mobile X-ray systems due to potential exposure time errors affecting diagnostic imaging. Affected units have serial numbers 00334-00361.
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.
Micro-X is recalling specific models of their Rover Mobile X-ray systems because the exposure time settings may not work correctly for diagnostic imaging. This could lead to images that aren't properly diagnostic, but it doesn: t cause immediate injury or danger to users.
The system's exposure time settings may not work correctly due to variations in hardware and how timers start. This can cause the x-ray images to be less diagnostic than intended, but it doesn't cause immediate injury or danger.
Medical facilities using the Micro-X Rover Mobile X-ray system with serial numbers 00334, 00348, 00349, 00351, or 00361 are affected. Staff and patients using these units may be at risk of receiving images that aren't properly diagnostic.
Check if your Micro-X Rover Mobile X-ray system has serial numbers 00334, 00348, 00349, 00351, or 00361. The product was sold with UDI-DI: 9357123000037.
Verify your Micro-X Rover Mobile X-ray system's serial number is one of 00334, 00348, 00349, 00351, or 00361.
The system's exposure time settings may not work correctly due to variations in hardware and how timers start, potentially causing images that aren't properly diagnostic.
Check your serial number against the list: 00334, 00348, 00349, 00351, or 00361. If affected, contact Micro-X for further instructions.
No, the recall is for potential imaging issues, not immediate injury or danger.
We’ve drafted a message you can send Micro-X to request your refund or repair — edit it as you like.
Subject: Recall Z-0664-2025 — Micro-X Micro-X Hello, I own a Micro-X that is covered by recall Z-0664-2025 from Micro-X. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
