Class II — Micro-X Ltd.
| Recalling firm | MICRO-X LTD |
|---|---|
| Registered facility | MICRO-X LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | X-Ray generator may malfunction resulting in the X-Ray being inoperable. |
| Product | Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71 |
| Quantity | 32 units |
| Distribution | US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto Rico. |
| Initiated | 2026-03-27 |
| Classified | 2026-04-22 |
| Recall number | Z-1918-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Micro-X Ltd. (Z-1918-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98644/
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