BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 2933097 · Received January 3, 2013

    Report

    Report Number
    1831750-2013-90035
    Event Type
    Malfunction
    Date Received
    January 3, 2013
    Date of Event
    December 7, 2012
    Report Date
    December 7, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LIFE-HERE LABELS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LIFT-HERE LABELS WERE ILLEGIBLE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3880 POWER PRO AMBULANCE COT WHEELED, STRETCHER FPO STRYKER MEDICAL 6500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1