Micro-X Ltd. recalls Rover Mobile X-ray Systems (model MXU-RV35) due to potential early x-ray tube failure from excessive thermal load. Affected units may require repair or replacement to prevent safety risks.
Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
Micro-X Ltd. is recalling Rover Mobile X-ray Systems (model MXU-RV35) because the x-ray tube may fail early due to overheating. This could lead to unsafe imaging during medical procedures if not addressed.
The x-ray tube in the Rover system may overheat during use, causing early failure. This could lead to unsafe imaging conditions if the system malfunctions during medical procedures.
Healthcare providers using the Rover Mobile X-ray System for medical imaging are most at risk. Patients receiving exams with the affected units could face potential safety issues.
Check for the model number MXU-RV35 on the device. The system is sold under the brand name Rover and is used for mobile medical imaging. Serial numbers include patterns like MSN0348 to MSN0438.
Look for the model number MXU-RV35 on the device label or documentation.
Reach out to Micro-X Ltd. for repair or replacement options if the device is affected.
The x-ray tube may fail early due to excessive thermal load, which could lead to unsafe imaging conditions during medical procedures.
Check the model number and contact Micro-X Ltd. for repair or replacement options if the device is affected.
The recall addresses potential x-ray tube failure, which could lead to unsafe imaging conditions, but the official notice does not specify injury risks.
We’ve drafted a message you can send Rover to request your refund or repair — edit it as you like.
Subject: Recall Z-1579-2025 — Rover Rover Hello, I own a Rover that is covered by recall Z-1579-2025 from Rover. 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.
