[Recalled] DR Systems Unity PACS software, now known as Merge Unity PACS software. — The software fails to associate to the correct MG image if there are two images… | FDA 2015-10-15
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | DR Systems Unity PACS software, now known as Merge Unity PACS software. |
|---|---|
| Brand / manufacturer | Merge Healthcare, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0939-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 15 October 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The software fails to associate to the correct MG image if there are two images for the same view.
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.