Merge Healthcare, Inc. recalls Merge OrthoPACS
- Recalling company
- Merge Healthcare, Inc.
- Product
- Merge OrthoPACS, 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 30, 2026
- Reported
- Aug 12, 2026
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, and UK.
- Status
- Ongoing
- Quantity
- 5 units
- Lot / codes
- UDI/DI (01)00842000101154(10)9.4.0.P02(11)260302, with Affected Versions: 9.4, 9.4 P01, and 9.4 P02.
- Company location
- Hartland, WI
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2875-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2875-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.