Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1918-2026 — Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71

U.S. FDA — Device Enforcement · Australia · 2026-03-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1918-2026
Date of alert
2026-03-27
Country / jurisdiction
Australia
Risk level
Class II
Risk type
recall
Brand
Micro-X Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
09357123000051
Reported risk: X-Ray generator may malfunction resulting in the X-Ray being inoperable.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.