Randox Laboratories Ltd.: Medical Device Recalls in 2022

According to to data from the FDA, there were 7 medical device recalls made by Randox Laboratories Ltd. in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD
• Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
• Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD
• CK MB Calibrator, Catalogue Number CK2393
• IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM in serum and plasma Catalog Number: IA3832
• The Randox Serology I Positive Control contains the following analytes in human based plasma: Anti HIV 1/2, Anti HTLV 1/2, Anti HCV, HBsAg, Anti HBc, and Anti Treponema pallidum IgG. The product is delivered as a liquid in a kit of 3 identical ready-to-use vials of 5 mL each.
• IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in serum and plasma Catalog Number: IM3834