Randox Laboratories Ltd. recalls Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053

Recall date

March 11, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1785-2019

FDA classification

Class II

Brand / firm

Randox Laboratories Ltd.

Sold / distributed

Product distributed to CA, DE, WV, and Puerto Rico.

Why it was recalled

Customers may observe a decrease in recovered concentration with regards to NTproBNP in the Liquid Cardiac Control lots identified, on the Siemens Dimension EXL LOCI.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053