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.
Read the official notice →- Date
- 2025-04-23
- Country
- United States
- Brand
- Micro-X
- Product
- Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV35 Product Description: Rover Mobile X-rays System…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of CA, NJ, and Puerto Rico (US…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2026-04-29
USMicro-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.
FDA · DeviceMicro-X Ltd.US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto…Official notice →- 2025-04-30
- 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 internal fastening mechanism within generator of mobile x-Ray to fail.
- 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
- 2025-04-23
- US
Stryker GmbH recalls Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;
The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
FDA · DeviceStryker GmbHUS Nationwide distribution in the states of CA, GA, IL, KY, MA, MD, NY, OH,…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) NAIL PACK, Model Number: SUT15830A;
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Canada, Mexico,…Official notice → - US
Channel Medsystems, Inc. recalls Brand Name: Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION, ENDOMETRIAL Model/Catalog Number: FGS-7000 Product…
Due to evaporator gasket not sealing which can cause liquid nitrous oxide to drip/leak from the bottom of the device handle during treatment or after treatment during venting of the device
FDA · DeviceChannel Medsystems, Inc.U.S Nationwide distribution in the states of AL, AZ, CA, CO, CT, DE, FL, GA,…Official notice → - US
Maquet Cardiovascular, LLC recalls Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).
Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.
FDA · DeviceMaquet Cardiovascular, LLCWorldwide - US Nationwide distribution in the states of AL, CA, CO, DC, FL,…Official notice → - US
Abbott Diagnostics Scarborough, Inc. recalls Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software…
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
- US
Abbott Diagnostics Scarborough, Inc. recalls Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software…
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
FDA · DeviceAbbott Diagnostics Scarborough, Inc.Worldwide distribution - US Nationwide and the countries of Australia;…Official notice →