[Recalled] vRad PACS with Mammography — The error resulted in intermittent failure of current (primary) radiology study… | FDA 2023-05-09
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | vRad PACS with Mammography |
|---|---|
| Brand / manufacturer | Virtual Radiologic Corp. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2235-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 09 May 2023 |
| EAN / barcode | 00862234000313 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.