FDA Device recall Z-2874-2026
Merge PACS, medical imaging diagnostic workstation
- FDA Device
- Class II
- ongoing
- Published 2026-08-12
On 2026-08-12 the FDA classified a Class II recall of Merge PACS, medical imaging diagnostic workstation by Merge Healthcare, citing thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2874-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-30 |
| Published | 2026-08-12 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Merge Healthcare |
| Distribution | US |
Product
Merge PACS, medical imaging diagnostic workstation
Reason
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
Identifiers
| code_info | UDI (01)00842000101215(10)9.4.0.P01(11)250916, (01)00842000101154(10)9.4.0.P02(11)260302 with Affected Versions: 9.4, 9.4 P01, and 9.4 P02. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2874-2026%22
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