---
title: "vRad PACS with Mammography — FDA record Z-2235-2023 | Is It on Recall"
description: "The error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist."
url: https://isitonrecall.com/recall/fda-device-z-2235-2023-vrad-pacs-with-mammography/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# vRad PACS with Mammography — FDA record Z-2235-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 9, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: vRad PACS with Mammography
- **Reason**: The error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist.
- **Classification**: Class II
- **Recalling firm**: Virtual Radiologic Corp.
- **Quantity**: 8 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2235-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2235-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | (01)00862234000313(10)23.2 Build 23.2.0.117 through (01)00862234000313(10) 23.4 Build 23.4.25.1 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [North Dakota](https://isitonrecall.com/state/north-dakota/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
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- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Aug 2, 2023
- **Recall initiation date**: May 9, 2023
- **Center classification date**: Jul 21, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2235-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Virtual Radiologic Corp. records](https://isitonrecall.com/brand/virtual-radiologic-corp/)
