Randox recalls Liquid Cardiac Controls with catalogue number CQ5053 due to reduced N-TproBNP recovery in recent batches. Affected units may have inaccurate cardiac test results.
Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue number CQ5053 due to an observed decrease in recovery for N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP) in recent lots.
Randox is recalling Liquid Cardiac Controls with catalogue number CQ5053 because recent batches show lower recovery rates for N-TproBNP, a key cardiac test marker. This could lead to inaccurate test results if used without the recall fix.
The recall is for a specific batch of the Liquid Cardiac Controls product. Recent lots have shown a decrease in recovery for N-TproBNP, which is a protein measured in cardiac tests. This could cause inaccurate test results if the product is used without the recall fix.
Healthcare professionals using Randox Liquid Cardiac Controls with catalogue number CQ5053 for cardiac testing. Those testing patients with heart conditions may be at slightly higher risk due to potential inaccuracies.
Check for catalogue number CQ5053 on the product label. The affected batches are 4245CK (exp. Nov 2019), 4248CK (exp. Nov 2019), 4313CK (exp. Jun 2020), and 4316CK (exp. Jun 2020).
Look for catalogue number CQ5053 and batch numbers 4245CK, 4248CK, 4313CK, or 4316CK on the product label.
Randox recalls Liquid Cardiac Controls with catalogue number CQ5053 due to reduced recovery rates for N-TproBNP in recent batches, which could lead to inaccurate cardiac test results.
Check the product label for catalogue number CQ5053 and batch numbers 4245CK, 4248CK, 4313CK, or 4316CK. If you have these, contact Randox for guidance.
The recall record does not specify a fix or remedy. Affected units should be checked and contacted for further instructions.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-0414-2020 — Randox Randox Hello, I own a Randox that is covered by recall Z-0414-2020 from Randox. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
