BEUDAMED
    8 results · 12ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Recall × Status: Open, Classified × Clear all

    Verigene CDF Nucleic Acid Test, Part No. 30-002-22

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OZN·June 17, 2022

    Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number: 20-006-022

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OCC·October 30, 2020

    VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-23

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code PCH·June 17, 2022

    Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code PCH·June 5, 2023

    VERIGENE Clostridium difficile Nucleic Acid Test, REF 30-002-022

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OZN·June 5, 2023

    K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013

    FDA Recall
    Open, Classified ·Kamiya Biomedical Company, LLC·Product code CFF·September 28, 2022

    V8 Immunodisplacement Kit REF 1803

    FDA Recall
    Open, Classified ·Helena Laboratories, Corp.·Product code CFF·April 6, 2022

    HUDSON RCI Addipak, UNIT DOSE VIALS, 5mL Sterile 0.9% NaCl Solution for Inhalation USP. REF RHUD59U

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code CAF·August 4, 2023