BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONTEC STERILE GLOVES

    MDR report key: 19127988 · Received April 16, 2024

    Report

    Report Number
    MW5153932
    Event Type
    Malfunction
    Date Received
    April 16, 2024
    Date of Event
    March 27, 2024
    Report Date
    April 12, 2024
    Manufacturer
    CONTEC, INC.
    Product Code
    LZC
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KS, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    DEAD BUG FOUND INLAYED IN STERILE GLOVE.

    Description of Event or Problem · 0

    ADDITIONAL INFORMATION IS RECEIVED ON 06/07/2024 FOR A REPORT NUMBER MW5153932.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    540373 CONTEC STERILE GLOVES PATIENT EXAMINATION GLOVE, SPECIALTY LZC CONTEC, INC. HCGS0022 CGN80/FKTPM 9600012-7

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown