BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PICKER

    MDR report key: 111579 · Received August 8, 1997

    Report

    Report Number
    MW1011853
    Event Type
    Malfunction
    Date Received
    August 8, 1997
    Date of Event
    August 8, 1997
    Report Date
    August 8, 1997
    Manufacturer
    PICKER INTL.
    Product Code
    EAJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    FOUR LEAD APRONS WERE MFG WITH RADIOACTIVE, CONTAMINATED MATERIAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PICKER LEAD APRON EAJ PICKER INTL. UNK UNK
    2 PICKER LEAD APRON EAJ PICKER INTL. UNK UNK
    3 PICKER LEAD APRON EAJ PICKER INTL. UNK UNK
    4 PICKER LEAD APRON EAJ PICKER INTL. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA