Class II — Merge Healthcare, Inc.
| Recalling firm | Merge Healthcare |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open. |
| Product | Merge OrthoPACS, medical imaging diagnostic workstation |
| Quantity | 5 units |
| Distribution | Worldwide distribution - US Nationwide and the countries of Canada, and UK. |
| Initiated | 2026-06-30 |
| Classified | 2026-08-04 |
| Recall number | Z-2875-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Merge Healthcare, Inc. (Z-2875-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99391/
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