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Randox Laboratories Ltd. recalls Liquid Cardiac Control, CQ5051
Recalled November 14, 2018 · FDA recall Z-0380-2019 · Randox Laboratories
Hazard
Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot 4245CK under REC334 on June 8, 2018. The firm has now confirmed the Liquid Cardiac Controls CQ5051, CQ5052 and CQ5053 are no longer suitable for the control of the Troponin T assay due to unacceptable variation between vials. · FDA Class II
Units
1763
Sold at
Distributed to IN, NY, PR, and WV.
Description
Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot 4245CK under REC334 on June 8, 2018. The firm has now confirmed the Liquid Cardiac Controls CQ5051, CQ5052 and CQ5053 are no longer suitable for the control of the Troponin T assay due to unacceptable variation between vials.
Product
Liquid Cardiac Control, CQ5051
Manufacturer(s)
Randox Laboratories Ltd.
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →