BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1080100 · Received July 17, 2008

    Report

    Report Number
    1831750-2008-00099
    Event Type
    Malfunction
    Date Received
    July 17, 2008
    Date of Event
    June 17, 2008
    Report Date
    June 17, 2008
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BRAKES ALLEGEDLY LOCKED UP WHILE A PT WAS ON A BED AND THE BED COULD NO LONGER BE MOVED. REPORTEDLY, THE PT HAD TO BE TRANSFERRED TO A STRETCHER FOR TRANSPORTATION. NO INJURY TO PT OR USER WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE II MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP, MEDICAL DIVISION 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK