BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 1883325 · Received October 20, 2010

    Report

    Report Number
    1831750-2010-03095
    Event Type
    Malfunction
    Date Received
    October 20, 2010
    Date of Event
    September 24, 2010
    Report Date
    September 24, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE FOOTEND LIFT WAS NOT OPERATIONAL. NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED AC POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIVISION 3002S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA