BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    30" TRANSPORT

    MDR report key: 1933105 · Received December 13, 2010

    Report

    Report Number
    1831750-2010-04767
    Event Type
    Malfunction
    Date Received
    December 13, 2010
    Date of Event
    November 16, 2010
    Report Date
    January 16, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE SIDE RAIL WILL NOT LOCK IN PLACE. INSPECTION SHOWED THE SIDE RAIL SPINDLE INSERT IS BROKEN. 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 30" TRANSPORT HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1004 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK