Reported Nov 27, 2019 · Terminated
Randox Liquid Cardiac Controls Catalogue Number CQ5051
Randox Laboratories, Limited
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, Limited · Ardmore; 55 The Diamond Road · Crumlin, N/A · N/A
Is this the product you have?
- Randox Liquid Cardiac Controls Catalogue Number CQ5051
- Lot codes and dates
- Catalogue NumberCQ5051
- GTIN05055273207446
- Batch/lot
4243CK (Exp. 28Nov2019)4246CK (Exp. 28Nov2019)4249CK (Exp. 28Nov2019)4260CK (Exp. 28Nov2019)4311CK (Exp. 28May2020)4317CK (Exp. 28May2020)
- Amount recalled
- 6,208
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Removal of claims for N-proBNP in the Liquid Cardiac Control model numbers CQ5051 due to an observed decrease in recovery for N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP) in recent lots.
This product could cause temporary or reversible health problems — stop using it.
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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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