Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71 — Class II medical device recall Z-1918-2026
Ongoing recall by Micro-X Ltd., reported 2026-04-29, distributed nationwide. X-Ray generator may malfunction resulting in the X-Ray being inoperable.
| Recall number | Z-1918-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Micro-X Ltd., Tonsley, N/A, Australia |
| Recall initiated | 2026-03-27 |
| Classified | 2026-04-22 |
| Reported by FDA | 2026-04-29 |
| Distributed | Nationwide (US) |
| Quantity | 32 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 09357123000037, 09357123000051 |
| Serial numbers | 223, 269, 334, 348, 349, 351, 359, 363, 384, 388, 391, 397, 399, 408, 413, 416, 419, 423, 425, 428, 429, 430, 431, 434, 435 and 8 more |
| Model numbers | MXU-RV35, MXU-RV71 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1918-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.