Z-2875-2026 Class II Ongoing
FDA device recall Z-2875-2026 was initiated by Merge Healthcare, Inc. on June 30, 2026 and is designated Class II. Reason for recall: Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open. The recall status is ongoing. Affected quantity: 5 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 12, 2026
- Initiation Date
- June 30, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5 units
Product Description
Merge OrthoPACS, medical imaging diagnostic workstation
Reason for Recall
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Canada, and UK.
Code Information
UDI/DI (01)00842000101154(10)9.4.0.P02(11)260302, with Affected Versions: 9.4, 9.4 P01, and 9.4 P02.