BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ATLAS

    MDR report key: 1962966 · Received December 22, 2010

    Report

    Report Number
    1831750-2010-05135
    Event Type
    Malfunction
    Date Received
    December 22, 2010
    Date of Event
    November 29, 2010
    Report Date
    November 29, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE PATIENT RIGHT FOOT SIDERAIL LATCH WELDMENT IS BROKEN. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ATLAS HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIVISION 0660 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK