BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1810633 · Received August 11, 2010

    Report

    Report Number
    1831750-2010-01791
    Event Type
    Malfunction
    Date Received
    August 11, 2010
    Date of Event
    July 8, 2010
    Report Date
    July 15, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: SCORPION KIT - BRACKETS FOR THE WHEELS THAT ASSIST WITH BRAKING.

    Description of Event or Problem · 1

    NA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NA