BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SPINBRUSH

    MDR report key: 799372 · Received December 20, 2006

    Report

    Report Number
    2280705-2006-00007
    Event Type
    Malfunction
    Date Received
    December 20, 2006
    Date of Event
    November 19, 2006
    Report Date
    December 19, 2006
    Manufacturer
    CHURCH & DWIGHT CO., INC.
    Product Code
    JEQ
    PMA / PMN Number
    exempt
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    PLEASE NOTE: CONSUMER HAS NOT RETURNED PRODUCT AND DID NOT IDENTIFY MODEL. DIFFERENT MODELS ARE MANUFACTURED AT DIFFERENT LOCATIONS. THE PRODUCT WAS MANUFACTURED AT ONE OF THE FOLLOWING LOCATIONS: CONTRACT MFR: KIN SENG MANUFACTURING CO., LTD. NO. 2-6 HINYIEH ROAD, XIA KANG SECTION, NANSHA ETDZ GUANGZHOU, PANYU, CHINA.

    Description of Event or Problem · 1

    BRUSH HANDLE EXPLODED AND BATTERY ACID GOT ALL OVER THE BATHROOM AND ON HER DAUGTHER. THE BATTERY ACID WAS REMOVED QUICKLY BY THE PARENTS. NO MEDICAL TREATMENT NECESSARY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SPINBRUSH TOOTHBRUSH, POWERED SEC 872.6865 (JEQ) JEQ CHURCH & DWIGHT CO., INC. UNK NA

    Patients

    Seq Age Sex Outcome Treatment
    1 15 YR