BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 1933281 · Received December 2, 2010

    Report

    Report Number
    1831750-2010-04355
    Event Type
    Malfunction
    Date Received
    December 2, 2010
    Date of Event
    November 30, 2010
    Report Date
    December 1, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    FLUID LEAK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE CUSTOMER THAT POWERPRO HAS TWO HYDRAULIC LEAKS. NO ADVERSE CONSEQUENCES OR INJURIES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1