BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LATEX GLOVE, LOW POWDER

    MDR report key: 10999 · Received January 21, 1994

    Report

    Report Number
    MW1000439
    Event Type
    Malfunction
    Date Received
    January 21, 1994
    Manufacturer
    CHESTER LABORATORIES, INC.
    Product Code
    LYY
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AR, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    LATEX GLOVES, BOTH MEDIUM AND LARGE ARE DEFECTIVE. ALMOST EVERY OTHER ONE HAS A HOLE OR TEAR IN IT AND EVEN HAVE FINGERS CRIMPED UP IN A WAD. THEY ALSO TEAR EASILY. DATE EVENT OCCURRED: 12/93. (ALSO SEE MEDWATCH 1000440.)

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LATEX GLOVE, LOW POWDER Implant LYY CHESTER LABORATORIES, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Other