Reported Jun 26, 2019 · Terminated

Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053

Randox Laboratories Ltd.

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: Randox Laboratories Ltd. · 55 Diamond Road · Crumlin (North), N/A · N/A

Is this the product you have?

    • Liquid Cardiac Control
    • Model Nos. CQ5051
    • CQ5052
    • CQ5053
Lot codes and dates
    • lots 4243CK
    • 4244CK
    • 4245CK
Amount recalled
11420 kits

Where it was sold

Why it was recalled

Customers may observe a decrease in recovered concentration with regards to NTproBNP in the Liquid Cardiac Control lots identified, on the Siemens Dimension EXL LOCI.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated May 15, 2020 · Data as of Sep 19, 4:53 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.