Brand

Merge Healthcare, Inc.: official recall notices

5 official recall or safety notices on this site name Merge Healthcare, Inc., dated between 2025-02-19 and 2025-08-11. They were issued by 1 authority: US FDA — Medical Devices (5).

Countries where the notices were issued: United States (5).

Name as written in the notices: Merge Healthcare, Inc.. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

Year	Notices
2025	5

Notices by authority

Authority	Notices
US FDA — Medical Devices	5

All notices

Date	Authority	Product	Hazard (as classified)
2025-08-11	US FDA — Medical Devices	Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The M	—
2025-02-19	US FDA — Medical Devices	VERICIS, Merge Cardio, Model/Catalog Number: Version 9.x, Software Version: 9.0.6 and 9.0.8; VERICIS is an integrated ca	—
2025-02-19	US FDA — Medical Devices	VERICIS, Merge Cardio, Model/Catalog Number: Version 10.x, Software Version: 10.0, 10.1.1.1, 10.1.2, 10.2.0, 10.2 P2 , 1	—
2025-02-19	US FDA — Medical Devices	Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.1, 12.1.1, 12.2, 12.3, 12.3.1, 12.3.2, 12.3.3, 12	—
2025-02-19	US FDA — Medical Devices	VERICIS, Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.0.1, 12.0.2; The VERICIS is an integrate	—

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