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

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 27, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

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
Recalling firm
Micro-X Ltd.
Quantity
32 units
Agency-reported status
Ongoing
Source record identifier
Z-1918-2026

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLot 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

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto Rico.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Apr 29, 2026
Recall initiation date
Mar 27, 2026
Center classification date
Apr 22, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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