Micro-X Ltd. recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
X-Ray generator may malfunction resulting in the X-Ray being inoperable.
Read the official notice →- Date
- 2026-04-29
- Country
- United States
- Brand
- Micro-X
- Product
- Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
- Classification
- Class II
- Units
- US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Micro-X recalls
- 2025-04-30
USMicro-X Ltd. recalls Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Description: Rover Mobile X-rays System…
Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
- 2025-04-23
- US
Micro-X Ltd. recalls Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV35 Product Description: Rover Mobile X-rays System…
Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
FDA · DeviceMicro-X Ltd.US Nationwide distribution in the states of CA, NJ, and Puerto Rico (US…Official notice → - 2024-12-18
- US
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV19
During internal testing it was found that if the system is Ready to expose and the hand switch is then dropped into the stowage unit such that it lands on the prep/expose switch, the prep switch can be activated for a…
- US
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV35; MICRO-X Rover Mobile X-ray System, # MXU-RV71
Mobile x-ray system can report and deliver a lower post-exposure mAs value than what set by the operator.
- US
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV35
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.
- 2024-12-04
- US
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV35
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…
Other drugs & medical recalls in the United States
- 2026-04-29
- US
Remel Europe Ltd. recalls Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O serotype as a 2-O serotype.
FDA · DeviceRemel Europe Ltd.Worldwide - US Nationwide distribution to the states of AL, CA, FL, IA, IL,…Official notice → - US
Beckman Coulter, Inc. recalls Access Total T4 Calibrator, Catalog No. 33805
Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product specifications. A false low patient result could cause a…
FDA · DeviceBeckman Coulter, Inc.Worldwide distribution - US Nationwide and the countries of Argentina,…Official notice → - US
Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space…
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of GA, OR, TN, and WA.Official notice → - US
ARROW INTERNATIONAL, LLC recalls MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code:…
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
FDA · DeviceARROW INTERNATIONAL, LLCU.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA,…Official notice → - US
ARROW INTERNATIONAL, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is…
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
FDA · DeviceARROW INTERNATIONAL, LLCU.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA,…Official notice → - US
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.
XXX
FDA · DeviceOlympus Corporation of the AmericasWorldwide distribution - US Nationwide and the countries of Canada, China,…Official notice →