BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRIME5TH/WHEEL ELECT STRETCHER

    MDR report key: 2870574 · Received November 14, 2012

    Report

    Report Number
    1831750-2012-11907
    Event Type
    Malfunction
    Date Received
    November 14, 2012
    Date of Event
    October 16, 2012
    Report Date
    October 16, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    MFR'S INVESTIGATION IS ONGOING. IF ADD'L INFO IS RECEIVED, A F/U REPORT MAY BE SUBMITTED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE FOOT END COULD NOT BE PUMPED UP. IT IS UNK WHETHER THERE WAS PT INVOLVEMENT OR ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRIME5TH/WHEEL ELECT STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1105000000E NA

    Patients

    Seq Age Sex Outcome Treatment
    1