FDA Device recall Z-2601-2017
Merge OrthoPACS software
- FDA Device
- Class II
- terminated
- Published 2017-06-28
On 2017-06-28 the FDA classified a Class II recall of Merge OrthoPACS software by Merge Healthcare, citing studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate via telmed protocol to the destination server and may fail to import on the destination server.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2601-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-24 |
| Published | 2017-06-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Merge Healthcare |
| Distribution | US |
Product
Merge OrthoPACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
Reason
Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate via telmed protocol to the destination server and may fail to import on the destination server.
Identifiers
| code_info | Versions 6.6, 6.6.1, 6.6.2, 6.6.2.1, and 6.6.2.2 |
|---|
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-2601-2017%22
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