Brand

Randox Laboratories Ltd.: official recall notices

7 official recall or safety notices published on this site name Randox Laboratories Ltd., dated between 2023-06-13 and 2024-04-05. They were issued by 1 authority: US FDA — Medical Devices (7).

Countries where the notices were issued: Ireland (7).

Name as written in the notices: Randox Laboratories Ltd.. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

What this page counts: the notices published as pages on product-guru.org, over every date (this site publishes a selection of the notices in the ProductGuru index). The brand scorecards count every indexed notice in a rolling 24-month window instead, so their totals differ from this page.

Notices by year

Year	Notices
2024	1
2023	6

Notices by authority

Authority	Notices
US FDA — Medical Devices	7

All notices

Date	Authority	Product	Hazard (as classified)
2024-04-05	US FDA — Medical Devices	Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative determination of parent drug molecule and	—
2023-11-29	US FDA — Medical Devices	RX Series Copper (Cu) Assay Ref. Number CU2340	—
2023-09-06	US FDA — Medical Devices	RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000	—
2023-09-06	US FDA — Medical Devices	RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000	—
2023-09-06	US FDA — Medical Devices	RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R (refurbished)	—
2023-07-19	US FDA — Medical Devices	Randox Liquid Protein Calibrators-SP CAL-(LIQ)-In vitro diagnostic product used for the calibration of ASO, Complement C	—
2023-06-13	US FDA — Medical Devices	Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) UR3825 (2) UR3873 (3) UR8334 (4) UR8070 (Modena	—

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