BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1222304-2016-00015

    MDR report key: 5463925 · Received February 26, 2016

    Report

    Report Number
    1222304-2016-00015
    Event Type
    Injury
    Date Received
    February 26, 2016
    Date of Event
    February 17, 2016
    Report Date
    February 17, 2016
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ON (B)(6) 2016: - THE CONSUMER HAS DISCARDED THE DEVICE. THEREFORE, AN EVALUATION WILL NOT BE POSSIBLE. CONSUMER HAS REQUESTED A REPLACEMENT. A REPLACEMENT WILL BE SENT TO THE CONSUMER ONCE PHOTOS OF PURCHASE HAS BEEN RECEIVED.

    Description of Event or Problem · 1

    ON (B)(6) 2016 - CONSUMER ALLEGES THE GLASS ON THE SCALE EXPLODED WHEN PLACED ON THE FLOOR. THE CONSUMER RECEIVED CUTS ON HANDS AND FEET. THE SCALE WAS DISCARDED. CONSUMER WILL SUBMIT PHOTOS AS PROOF OF PURCHASE. THE CONSUMER HAS REQUESTED A REPLACEMENT.

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Other