BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRIME 5TH WHEEL STRETCHER, 30"

    MDR report key: 2221429 · Received August 16, 2011

    Report

    Report Number
    1831750-2011-08709
    Event Type
    Malfunction
    Date Received
    August 16, 2011
    Date of Event
    July 19, 2011
    Report Date
    July 19, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD END WOULD NOT LOWER ON THE STRETCHER. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRIME 5TH WHEEL STRETCHER, 30" HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1102000030 NA

    Patients

    Seq Age Sex Outcome Treatment
    1