← FDA ENFORCEMENT
Z-2874-2026Class II

Merge Healthcare, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Merge Healthcare, Inc.
Product type
Device
Status
Ongoing
Report date
2026-08-12
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, and UK.
Firm state
WI
Product quantity
53 units
Initiated by
Voluntary: Firm initiated
Reason for recall

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Product description

Merge PACS, medical imaging diagnostic workstation

Code / lot info

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.

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →