Z-2874-2026 Class II Ongoing

Recalled by Merge Healthcare, Inc. — Hartland, WI

FDA device recall Z-2874-2026 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: 53 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
53 units

Product Description

Merge PACS, 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 (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.