[Recalled] DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a variety of diagnostic imagi |
|---|---|
| Brand / manufacturer | Merge Healthcare, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1385-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 08 April 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The software is not adding the correct tomo image.
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 →
Related recalls from Merge Healthcare, Inc.
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.
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