BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONAIR

    MDR report key: 6033147 · Received October 17, 2016

    Report

    Report Number
    1222304-2016-00041
    Event Type
    Injury
    Date Received
    October 17, 2016
    Date of Event
    September 17, 2016
    Report Date
    September 19, 2016
    Manufacturer
    CONAIR CORPORATION
    Product Code
    MNW
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ON 10/17/2016 - WE HAVE REQUESTED THE DEVICE BE RETURNED TO THE MANUFACTURER. TO DATE, WE HAVE NOT RECEIVED THE DEVICE.

    Additional Manufacturer Narrative · 1

    ON 10/17/2016, WE HAVE REQUESTED THE DEVICE BE RETURNED TO THE MANUFACTURER. TO DATE, WE HAVE NOT RECEIVED THE DEVICE. ON (B)(6) 2017 ADDED THE UPC CODE TO THE SUPPLEMENTAL EMDR. DEVICE NOT RETURNED TO MANUFACTURER.

    Additional Manufacturer Narrative · 1

    ON 10/17/2016 - WE HAVE REQUESTED THE DEVICE BE RETURNED TO THE MANUFACTURER. TO DATE, WE HAVE NOT RECEIVED THE DEVICE. ON 1/31/2017 - ADDED THE UPC CODE TO THE SUPPLEMENTAL EMDR. ON 2/15/2017 - MANUFACTURERS NARRATIVE: THE PRODUCT WAS RECEIVED IN THE CONDITION THAT DEEMS IMPOSSIBLE TO PERFORM TESTING DUE TO THE SHATTERED GLASS. THIS OCCURENCE RARELY HAPPENS WITH THIS PRODUCT.

    Description of Event or Problem · 1

    ON 10/17/2016 - THE CONSUMERS GRANDDAUGHTER ALLEGEDLY DROPPED A BOTTLE ON THE PRODUCT WHICH CAUSE THE GLASS TO SHATTER. THE CONSUMERS GRANDDAUGHTER RECEIVED CUTS ON LEG. NO MEDICAL ATTENTION WAS REQUIRED.

    Description of Event or Problem · 1

    ON (B)(6) 2016, THE CONSUMERS GRANDDAUGHTER ALLEGEDLY DROPPED A BOTTLE ON THE PRODUCT WHICH CAUSE THE GLASS TO SHATTER. THE CONSUMERS GRANDDAUGHTER RECEIVED CUTS ON LEG. NO MEDICAL ATTENTION WAS REQUIRED.

    Description of Event or Problem · 1

    (B)(6) 2016 - THE CONSUMER'S GRAND DAUGHTER ALLEGEDLY DROPPED A BOTTLE ON THE PRODUCT WHICH CAUSE THE GLASS TO SHATTER. THE CONSUMER'S GRAND DAUGHTER RECEIVED CUTS ON LEG. NO MEDICAL ATTENTION WAS REQUIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    685304 CONAIR BMI SCALE MNW CONAIR CORPORATION WW78

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Other