BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIOHAZARD BAGS 6 X 9

    MDR report key: 12568957 · Received October 1, 2021

    Report

    Report Number
    MW5104344
    Event Type
    Malfunction
    Date Received
    October 1, 2021
    Report Date
    September 29, 2021
    Manufacturer
    MEDLINE INDUSTRIES, INC.
    Product Code
    NNK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    SMALL BUGS FOUND IN MULTIPLE 6 X 9 BIOHAZARD BAGS FROM MAIN OPERATING ROOM DISTRIBUTION. REF DYND30261, REORDER NUMBER (B)(4). FDA SAFETY REPORT ID # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1463399 BIOHAZARD BAGS 6 X 9 CONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE NNK MEDLINE INDUSTRIES, INC. REF DYND30261

    Patients

    Seq Age Sex Outcome Treatment
    1