BEUDAMED
    FDA Adverse Event Summary report: N

    GYNNIE OB/GYN STRETCHER

    MDR report key: 1213463 · Received October 20, 2008

    Report

    Report Number
    1831750-2008-00142
    Date Received
    October 20, 2008
    Date of Event
    September 22, 2008
    Report Date
    October 17, 2008
    Manufacturer
    STRYKER CORP-MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    VISUAL INSPECTION INDICATES LIKELY CUSTOMER MISUSE.

    Description of Event or Problem · 1

    IT WAS REPORTED A CUSTOMER ORDERED CALF SUPPORTS AND ONE OF THEM BROKE WHEN THEY APPLIED WEIGHT TO IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GYNNIE OB/GYN STRETCHER STRETCHER FPO STRYKER CORP-MEDICAL 1061 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK