Randox Laboratories, Limited
10 recalls on record · Latest: Jan 29, 2025
FDA Devices Moderate Jan 29, 2025
Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers. Catalog Number: LP2757
FDA Devices Moderate Jan 29, 2025
Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers. Catalog Number: LP3403
FDA Devices Moderate Mar 4, 2020
RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random access, clini…
FDA Devices Moderate Nov 27, 2019
Randox Liquid Cardiac Controls Catalogue Numbers CQ5053.
FDA Devices Moderate Nov 27, 2019
Randox Liquid Cardiac Controls Catalogue Number CQ5051
FDA Devices Low Nov 20, 2019
RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343, GTIN: 5055273203066.
FDA Devices Moderate Aug 14, 2019
Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of…
FDA Devices Low Aug 14, 2019
Assayed Bovine Multi-Sera Level 1, Model No. AL1027
FDA Devices Moderate Jul 31, 2019
RX Daytona, Model Nos. RX4040 and RX4041
FDA Devices Moderate Dec 14, 2016