Reported Mar 29, 2017 · Terminated

Merge Cardio software.

Merge Healthcare, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Merge Healthcare, Inc. · 900 Walnut Ridge Dr · Hartland, WI · 53029-8347

Is this the product you have?

  • Merge Cardio software.
Lot codes and dates
    • Versions 9.0
    • 9.0.1
    • 9.0.2
    • 9.0.3
    • 9.0.4
    • 9.0.5
    • 9.0.6
    • 9.0.7
    • 9.0.8
    • 9.0.9
    • 10.0
    • 10.0.1
    • 10.1
    • 10.1.1
    • and 10.1.2
Amount recalled
217 sites potentially have the affected versions

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

Cardio study list does not show STAT studies without refreshing.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 26, 2019 · Data as of Sep 19, 6:51 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.