Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Randox Liquid Cardiac Controls Catalogue Number CQ5052. Recalled by Randox Laboratories, Limited Due to Removal of claims for N-proBNP in the Liquid...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Randox Laboratories, Limited directly.
Affected Products
Randox Liquid Cardiac Controls Catalogue Number CQ5052.
Quantity: 7,505
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 9 states: CA, CO, DE, GA, IN, MD, NJ, NY, WV
About Randox Laboratories, Limited
Randox Laboratories, Limited has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report