Warning
Micro-X Ltd. Recalls Rover Mobile X-ray System Model/Catalog Number:.
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:.
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.
Sources: FDA openFDA Enforcement Database