Official recall record

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

US FDA — Medical Devices · 2024-10-22 · AustraliaClass II

Issuing authority: US FDA — Medical Devices
Alert date: 2024-10-22
Country of alert: Australia
Alert level: Class II
Alert type: recall
Barcode (EAN/GTIN): 9357123000037
Brand on record: Micro-X Ltd.
Product category: Medical Device

What the authority reported

Mobile x-ray system receiving/storage(operation) requirements to be followed: Temp:14 to 131(50 to 86) degrees F, RH:10% to 86%(30% to 60%) allow condensation dry time, Atmospheric Pressure:50kPa to 106 kPa(70kPa to 106kPa), Altitude:-102ft to 12,000 ft, (Maximum Gradient:9 degrees Fahrenheit), which mitigate risk of capacitor malfunction, unpredictable behavior, overheating, unintended start-up.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · Australia · all filters

Same barcode in other registries

The same EAN appears in 2 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

2023-11-28 · US FDA — Medical Devices
MICRO-X Rover Mobile X-ray System, # MXU-RV35; MICRO-X Rover Mobile X-ray System, # MXU-RV71
2023-05-31 · US FDA — Medical Devices
MICRO-X Rover Mobile X-ray System, # MXU-RV35

Other recalls from this brand

2024-10-23 · US FDA — Medical Devices
MICRO-X Rover Mobile X-ray System, # MXU-RV19

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.