BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUIDEL LYRA DIRECT SARS-COV-2 ASSAY (M124)

    MDR report key: 11698410 · Received April 20, 2021

    Report

    Report Number
    1000122536-2021-00013
    Event Type
    Malfunction
    Date Received
    April 20, 2021
    Date of Event
    December 17, 2020
    Report Date
    April 20, 2021
    Manufacturer
    QUIDEL CORPORATION
    Product Code
    QJR
    UDI-DI
    30014613339144
    PMA / PMN Number
    EUA200423
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    FALSE POSITIVE: CUSTOMER REPORTED FP RESULTS ON LYRA DIRECT SARS; 7500 FAST DX RUN FILES PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    589601 QUIDEL LYRA DIRECT SARS-COV-2 ASSAY (M124) LYRA DIRECT SARS-COV-2 ASSAY QJR QUIDEL CORPORATION Coronavirus 30014613339144

    Patients

    Seq Age Sex Outcome Treatment
    1