Home / Recalls / Medical Devices
Randox Laboratories Ltd. recalls Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053
Recalled June 26, 2019 · FDA recall Z-1785-2019 · Randox Laboratories
Hazard
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. · FDA Class II
Units
11420 kits
Sold at
Product distributed to CA, DE, WV, and Puerto Rico.
Description
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.
Product
Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053
Manufacturer(s)
Randox Laboratories Ltd.
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →