Micro-X Ltd. recalls Rover Mobile X-ray System
- Recalling company
- Micro-X Ltd.
- Product
- Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
- Reason
- X-Ray generator may malfunction resulting in the X-Ray being inoperable.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 27, 2026
- Reported
- Apr 29, 2026
- Distribution
- US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto Rico.
- Status
- Ongoing
- Quantity
- 32 units
- Lot / codes
- Lot Code: Refer to product traceability spreadsheet provided MXU-RV71 UDI: (01)09357123000051/ Serial Numbers: 334 397 399 408 423 425 459 MXU-RV35 UDI: (01)09357123000037/ Serial Numbers: 269 223 349 348 351 363 388 384 391 359 416 419 428 429 430 431 435 434 436 413 437 438 460 461 462
- Company location
- Tonsley, N/A
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1918-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1918-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.