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Agilent Technologies Recalls
5 recalls on record · April 12, 2017 to April 16, 2025 · Medical Devices
Recalls by year
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25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 16, 2025Medical DevicesFDA
Agilent Technologies, Inc. recalls GenetiSure Dx Labeling Kit, REF: K1201-64105, contains human reference DNA female aliquot, REF5190-7317. A required kit
Hazard: DNA Labeling Kit for use in sample labeling to be hybridized to oligonucleotide microarrays has a component, Human Reference DNA Female aliquot, affected by a mosaic aberration that may result in Chromosome 12 baseline shift, which may lead to false positive/negative results, resulting in diagnosis delay, and may lead to delayed treatment of a treatable genetic disorder.
June 5, 2024Medical DevicesFDA
Agilent Technologies recalls Brand Name: Dako CoverStainer, Dako CoverStainer CPO Product Name: CoverStainer, CoverStainer CPO Model/Catalog Number
Hazard: There is the potential for the front plexiglass door of the automated slide processing system to break causing potential injury.
July 20, 2022Medical DevicesFDA
Agilent Technologies, Inc. recalls Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omn
Hazard: Label provided for substrate vail contained incorrect expiration date.
September 4, 2019Medical DevicesFDA
Agilent Technologies, Inc. recalls MassHunter Quantitative Analysis Software, Version B.07.01, used with Triple Quadrupole Mass Spectrometers, models K6460
Hazard: When utilizing specific software versions of an LC/MS device, and Batch at a Glance in Compound Table view, a defect occurs when a new sample(s) is inserted. This defect creates a mismatch between the sample name and the column header whereby the sample header will be offset by one sample. The recalling firm requests that you discontinue using this workflow to generate reports because the Quant batch table will not display fully analyzed results or save any changes made.
April 12, 2017Medical DevicesFDA
Agilent Technologies, Inc. recalls Bond Elut OMS (Dried Matrix Spotting)' Product; Catalog model numbers: 5022-8226 - Auto DBS Card (LCMS Extraction Sy
Hazard: The product was marketed without 510(k) clearance.