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Randox Laboratories Ltd. recalls RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000
Recalled November 8, 2023 · FDA recall Z-0202-2024 · Randox Laboratories
Hazard
RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may result i issues with the re-run feature conditions when incorrectly. Potential to report incorrectly. · FDA Class II
Units
13 units
Sold at
US Nationwide distribution including Puerto Rico
Description
RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may result i issues with the re-run feature conditions when incorrectly. Potential to report incorrectly.
Product
RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000
Manufacturer(s)
Randox Laboratories Ltd.
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →