FDA Device recall Z-2235-2023
vRad PACS with Mammography
- FDA Device
- Class II
- ongoing
- Published 2023-08-02
On 2023-08-02 the FDA classified a Class II recall of vRad PACS with Mammography by Virtual Radiologic, citing the error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2235-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-05-09 |
| Published | 2023-08-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Virtual Radiologic |
| Distribution | US |
Product
vRad PACS with Mammography
Reason
The error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist.
Identifiers
| code_info | (01)00862234000313(10)23.2 Build 23.2.0.117 through (01)00862234000313(10) 23.4 Build 23.4.25.1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2235-2023%22
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