FDA Device recall Z-0939-2017
DR Systems Unity PACS software, now known as Merge Unity PACS software
- FDA Device
- Class II
- terminated
- Published 2017-01-11
On 2017-01-11 the FDA classified a Class II recall of DR Systems Unity PACS software, now known as Merge Unity PACS software by Merge Healthcare, citing the software fails to associate to the correct MG image if there are two images for the same view.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0939-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-10-15 |
| Published | 2017-01-11 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Merge Healthcare |
| Distribution | CA, MT, PA, TX |
Product
DR Systems Unity PACS software, now known as Merge Unity PACS software.
Reason
The software fails to associate to the correct MG image if there are two images for the same view.
Identifiers
| code_info | Version 11.0 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0939-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.