BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1032433 · Received April 16, 2008

    Report

    Report Number
    1831750-2008-00059
    Event Type
    Malfunction
    Date Received
    April 16, 2008
    Date of Event
    March 13, 2008
    Report Date
    March 17, 2008
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FNL
    Removal / Correction Number
    1831750-2007-003
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BRAKES WERE NOT FUNCTIONING PROPERLY ON THIS BED. NO INJURY TO PATIENT 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