# FDA recall Z-2235-2023

> **Virtual Radiologic Corp.** · Class II · device recall initiated 2023-05-09.

## Product

vRad PACS with Mammography

## Reason for recall

The error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist.

## Distribution

US Nationwide distribution in the states of MD, MN, TN, FL, GA, TX, OK.

## Key facts

- **Recall number:** Z-2235-2023
- **Recalling firm:** Virtual Radiologic Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-09
- **Report date:** 2023-08-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Eden Prairie, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2235-2023

## Citation

> AI Analytics. FDA recall Z-2235-2023. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-2235-2023. Source: US FDA. Licensed CC0.

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