BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIG WHEEL STRETCHER, 30" LITTER

    MDR report key: 1902430 · Received November 12, 2010

    Report

    Report Number
    1831750-2010-03709
    Event Type
    Malfunction
    Date Received
    November 12, 2010
    Date of Event
    October 15, 2010
    Report Date
    October 15, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISON
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END JACK IS LEAKING OIL. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIG WHEEL STRETCHER, 30" LITTER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL DIVISON 1115000030 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA