BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SEVENTH GENERATION

    MDR report key: 13233737 · Received January 11, 2022

    Report

    Report Number
    1648563-2022-00001
    Event Type
    Malfunction
    Date Received
    January 11, 2022
    Date of Event
    November 23, 2021
    Report Date
    January 11, 2022
    Manufacturer
    FEMPRO CONSUMER PRODUCTS ULC
    Product Code
    HHD
    UDI-DI
    00732913450008
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    CONSUMER FOUND FOREIGN OBJECT IN MENSTRUAL PAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    9452 SEVENTH GENERATION MAXI PAD, REGULAR HHD FEMPRO CONSUMER PRODUCTS ULC 68525785 01131FP06 12:52:47 00732913450008

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown