Notice names this product. Micro-X’s Rover Mobile X-ray System Model/Catalog Number is named in FDA Class II recall Z-1918-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: X-Ray generator may malfunction resulting in the X-Ray being inoperable. Identifying details: 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. Units affected: 32 units. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
X-Ray generator may malfunction resulting in the X-Ray being inoperable.
Company / brand: Micro-X recalls
Affected product: Rover Mobile X-ray System Model/Catalog Number recall status
Official ID Z-1918-2026 · Official record ↗
Found something wrong or missing? Report a data error.
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.