Randox recalls Liquid Cardiac Controls CQ5052 due to reduced N-Terminal Pro-Brain Natriuretic Peptide recovery in recent batches. Affected units have specific batch numbers and expiration dates.
Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue number CQ5052 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 CQ5052 because recent batches show lower recovery rates for N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP). This could affect test accuracy for cardiac health monitoring. The recall affects specific batch numbers and expiration dates.
The product has a known issue where recent batches show decreased recovery of N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP). This means test results for cardiac health monitoring may be less accurate than expected, potentially leading to incorrect health assessments.
Healthcare professionals using Randox Liquid Cardiac Controls CQ5052 for cardiac testing are affected. Those using the product with batch numbers 4244CK, 4247CK, 4261CK, 4312CK, or 4315CK (expiring Nov 2019 or Jun 2020) are most at risk.
Check the product's catalogue number (CQ5052) and batch numbers: 4244CK, 4247CK, 4261CK, 4312CK, or 4315CK. These units expire by November 2019 or June 2020.
Verify the catalogue number and batch numbers listed in the product description.
Randox recalls Liquid Cardiac Controls CQ5052 due to observed decreased recovery of N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP) in recent batches.
Batch numbers 4244CK, 4247CK, 4261CK, 4312CK, and 4315CK (expiring November 2019 or June 2020).
No action is required for users with unaffected batches. Only specific batch numbers are affected.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-0413-2020 — Randox Randox Hello, I own a Randox that is covered by recall Z-0413-2020 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.
