BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6083 AMBULANCE COT

    MDR report key: 2070341 · Received April 18, 2011

    Report

    Report Number
    1831750-2011-03703
    Event Type
    Malfunction
    Date Received
    April 18, 2011
    Date of Event
    March 16, 2011
    Report Date
    March 22, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    WELD ON UPPER LIFT TUBE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE UPPER WELDMENT WAS CRACKED AROUND THE UPPER LIFT TUBE. THERE WAS NO REPORTED PT INVOLVEMENT OR ADVERSE CONSEQUENCES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 6083 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL 6083 NA

    Patients

    Seq Age Sex Outcome Treatment
    1