FDAClass IIApril 29, 2026

Rover Mobile X-ray System recall

Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71

Why was Rover Mobile X-ray System recalled?

X-Ray generator may malfunction resulting in the X-Ray being inoperable.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
Recalling firm
Micro-X Ltd.
Quantity
32 units
Distribution
US Nationwide distribution in the states and territories of WA, NJ, CA, Puerto Rico.
Recall date
April 29, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls