Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom
This page shows every FDA and USDA recall linked to Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
13
Total Recalls
2016
First Recall
2025
Most Recent
Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers...
Jan 23, 2025
· Device
Active
Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers....
Jan 23, 2025
· Device
Active
RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage:
A...
Feb 24, 2020
· Device
Terminated
Randox Liquid Cardiac Controls Catalogue Number CQ5052.
Oct 4, 2019
· Device
Terminated
Randox Liquid Cardiac Controls Catalogue Number CQ5051
Oct 4, 2019
· Device
Terminated
Randox Liquid Cardiac Controls Catalogue Numbers CQ5053.
Oct 4, 2019
· Device
Terminated
RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343, GTIN: 5055273203066.
Sep 23, 2019
· Device
Terminated
RX Imola, Model Nos. RX4900
Jun 24, 2019
· Device
Terminated
RX Daytona, Model Nos. RX4040 and RX4041
Jun 24, 2019
· Device
Terminated
Human Assayed Multi-Sera Level 2, Model NO. HN1530
Product Usage: This product is intended for in vitro diag...
Jun 11, 2019
· Device
Terminated
Assayed Bovine Multi-Sera Level 1, Model No. AL1027
Jun 10, 2019
· Device
Terminated
Liquid Cardiac Control CQ5053
Aug 8, 2017
· Device
Terminated
Magnesium on RX Imola analyser
IVD
Apr 14, 2016
· Device
Terminated