BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SPINBRUSH? PROCLEAN? POWERED TOOTHBRUSH

    MDR report key: 3178282 · Received June 19, 2013

    Report

    Report Number
    2280705-2013-00041
    Event Type
    Injury
    Date Received
    June 19, 2013
    Report Date
    June 19, 2013
    Manufacturer
    CHURCH & DWIGHT CO., INC.
    Product Code
    JEQ
    PMA / PMN Number
    EXEMPT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE EVENT OCCURRED AROUND (B)(6) 2013. LOT NUMBER FOR HANDLE: DD0110F2. LOT NUMBER FOR HEAD: DD0111H2. MANUFACTURING DATE FOR HANDLE: 04/20/2010. MANUFACTURING DATE FOR HEAD: 04/21/2010.

    Description of Event or Problem · 1

    CONSUMER REPORTED SHE CHIPPED HER TOOTH WHILE USING THE TOOTHBRUSH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    277636 SPINBRUSH? PROCLEAN? POWERED TOOTHBRUSH TOOTHBRUSH, POWERED JEQ CHURCH & DWIGHT CO., INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other