Brand

Randox Laboratories, Limited Recalls

9 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Randox Laboratories, Limited.

9Total Recalls
0Critical
17,378Units Affected
Dec 20, 2024Most Recent
All Recalls

Every Randox Laboratories, Limited Recall

Sorted by most recent. Click any recall for full details.

9 recalls
High RiskFDA
Randox Laboratories, Limited
Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers. Catalog Number: LP2757
Diagnostic Devices·33 affected·Dec 20, 2024
High RiskFDA
Randox Laboratories, Limited
Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers. Catalog Number: LP3403
Diagnostic Devices·15 affected·Dec 20, 2024
High RiskFDA
Randox Laboratories, Limited
RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random a...
Medical Devices·4,040 affected·Dec 19, 2019
High RiskFDA
Randox Laboratories, Limited
Randox Liquid Cardiac Controls Catalogue Numbers CQ5053.
Cardiac Devices·6,702 affected·Oct 4, 2019
High RiskFDA
Randox Laboratories, Limited
Randox Liquid Cardiac Controls Catalogue Number CQ5051
Cardiac Devices·6,208 affected·Oct 4, 2019
RecallFDA
Randox Laboratories, Limited
RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343, GTIN: 5055273203066.
Medical Devices·212 affected·Sep 23, 2019
High RiskFDA
Randox Laboratories, Limited
Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use, in the qualit...
Diagnostic Devices·149 affected·Jun 11, 2019
RecallFDA
Randox Laboratories, Limited
Assayed Bovine Multi-Sera Level 1, Model No. AL1027
Diagnostic Devices·4 affected·Jun 10, 2019
High RiskFDA
Randox Laboratories, Limited
Magnesium on RX Imola analyser IVD
Medical Devices·15 affected·Apr 14, 2016