FDA Device recall Z-1918-2026
Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
- FDA Device
- Class II
- ongoing
- Published 2026-04-29
On 2026-04-29 the FDA classified a Class II recall of Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71 by Micro X, citing X-Ray generator may malfunction resulting in the X-Ray being inoperable.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1918-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-03-27 |
| Published | 2026-04-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Micro X |
| Distribution | US |
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.
Identifiers
| code_info | Lot Code: Refer to product traceability spreadsheet provided MXU-RV71 UDI: (01)09357123000051/ Serial Numbers: 334 397…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1918-2026%22
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