BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ST104 TRANSPORT

    MDR report key: 2861162 · Received November 2, 2012

    Report

    Report Number
    1831750-2012-11467
    Event Type
    Malfunction
    Date Received
    November 2, 2012
    Date of Event
    October 12, 2012
    Report Date
    October 12, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKES WERE ALLEGEDLY NOT HOLDING; HOWEVER, STRYKER TECHNICIAN COULD NOT DUPLICATE THE EVENT. THE PRODUCT MEETS AND PERFORMS TO SPECIFICATION. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ST104 TRANSPORT HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0737 NA

    Patients

    Seq Age Sex Outcome Treatment
    1