Reported Nov 27, 2019 · Terminated
Randox Liquid Cardiac Controls Catalogue Number CQ5052.
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 CQ5052.
- Lot codes and dates
- Catalogue NumberCQ5052
- GTIN05055273207453
- Batch/lot4244CK (Exp. 28Nov2019), 4247CK (Exp. 28Nov2019), 4261CK (Exp. 28Nov2019), 4312CK Exp. 28Jun2020) and 4315CK (Exp. 28Jun2020)
- Amount recalled
- 7,505
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 catalogue number CQ5052 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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