# FDA recall Z-1786-2022

> **Micro-X Ltd.** · Class II · device recall initiated 2022-08-31.

## Product

MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19

## Reason for recall

Software calibration error with product equip with a Dose Area Product (DAP) meter.  This results in the product displaying the incorrect DAP meter values which may impede radiation exposure management decisions

## Distribution

Worldwide distribution - U.S. Nationwide distribution in the states of CA, NV, NY, OH, TX and WA and the countries of Australia, France, Israel, Japan, and United Arab Emirates.

## Key facts

- **Recall number:** Z-1786-2022
- **Recalling firm:** Micro-X Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-08-31
- **Report date:** 2022-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tonsley, N/A, Australia

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1786-2022

## Citation

> AI Analytics. FDA recall Z-1786-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1786-2022. Source: US FDA. Licensed CC0.

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