BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1660585 · Received April 12, 2010

    Report

    Report Number
    1831750-2010-00699
    Event Type
    Malfunction
    Date Received
    April 12, 2010
    Date of Event
    March 15, 2010
    Report Date
    March 15, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THERE ARE BRAKE HOLDING ISSUES, AND THE BRAKE FORCE ISN' HOLDING. NO ADVERSE CONSEQUENCE 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