BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRETCHER CHAIR

    MDR report key: 1942779 · Received December 10, 2010

    Report

    Report Number
    1831750-2010-04741
    Event Type
    Malfunction
    Date Received
    December 10, 2010
    Date of Event
    November 15, 2010
    Report Date
    November 15, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER IS BENT. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRETCHER CHAIR HOSPITAL WHEELED STRETCHER FPP STRYKER CORP., MEDICAL DIV. 5050 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK