BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 2 MED/SURGEBED

    MDR report key: 2061884 · Received March 18, 2011

    Report

    Report Number
    1831750-2011-02597
    Event Type
    Malfunction
    Date Received
    March 18, 2011
    Date of Event
    February 24, 2011
    Report Date
    February 24, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED WOULD ACT ERRATICALLY WHEN IT WAS PLUGGED IN, AND THEN IT WOULD NOT WORK AT ALL. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 2 MED/SURGEBED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1