Warning
Micro-X Ltd. Recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-1918-2026Medical Device
Micro-X Ltd. Recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35
Micro-X Ltd. · Class II — Moderate Risk
Product Description
Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
Reason for Recall
X-Ray generator may malfunction resulting in the X-Ray being inoperable.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto Rico.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Micro-X Ltd. has recalled a medical device that the FDA classified as Class II affecting 32 units. The recall was initiated on March 27, 2026. X-Ray generator may malfunction resulting in the X-Ray being inoperable. It was distributed nationwide. Class II recalls involve products that might cause a temporary health problem or pose only a slight threat of a serious nature. Consumers should discontinue use and contact the firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Medical Device Defects.