Randox Laboratories recalls

6 recalls on record · latest: February 1, 2023

Official U.S. recall history for Randox Laboratories, compiled from official government records.

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Randox Laboratories recalls CRP Immunoturbidimetric reagent. Intended for the quantitative in vitro determination of CRP concentration in serum Cat…

February 1, 2023 · Medical device recalls Moderate risk The Antibody (R2 reagent) is showing a positive bias compared to previous batch…

Randox Laboratories recalls RX Imola (RX4900) For Professional Use for the quantitative in vitro determination of various clinical chemistry tests.

May 4, 2018 · Medical device recalls Moderate risk Abnormal premature termination of the software could affect the use of the anal…

Randox Laboratories recalls Immunoassay Premium Controls (3x4x5mL and 12x5mL packages)

August 11, 2017 · Medical device recalls The ACTH in Immunoassay Premium and Premium Plus quality control does not meet…

Randox Laboratories recalls Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages)

August 11, 2017 · Medical device recalls The ACTH in Immunoassay Premium and Premium Plus quality control does not meet…

Randox Laboratories recalls Liquid Urine Control Level 3 For Professional Use in the quality control monitoring of In-Vitro Diagnostic Urinary Clin…

April 27, 2017 · Medical device recalls According to Randox Laboratories an investigation indicates a labelling error f…

Randox Laboratories recalls The Randox Liquid Cardiac Controls Level 1, Level 2, and Level 3 are liquid controls containing BNP, CK MB Mass, Digoxi…

September 16, 2016 · Medical device recalls Moderate risk An internal real-time stability monitoring program revealed decreased recovery…