BEUDAMED
    FDA Adverse Event Other Summary report: N

    SENSICARE POWDERFREE VINYL GLOVES

    MDR report key: 273070 · Received April 10, 2000

    Report

    Report Number
    9615361-2000-00004
    Event Type
    Other
    Date Received
    April 10, 2000
    Date of Event
    March 30, 2000
    Report Date
    April 7, 2000
    Manufacturer
    MAXXIM MEDICAL CANADA, LTD.
    Product Code
    LYZ
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    RN'S HANDS DEVELOPED AREAS OF REDNESS AFTER REMOVING GLOVES FROM HANDS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SENSICARE POWDERFREE VINYL GLOVES NON STERILE POWDERFREE MEDICAL EXAMINATION GLOVES LYZ MAXXIM MEDICAL CANADA, LTD. NA 922UB13

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other