BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CAMA SECURE II-REGULAR

    MDR report key: 2091040 · Received May 11, 2011

    Report

    Report Number
    1831750-2011-04551
    Event Type
    Malfunction
    Date Received
    May 11, 2011
    Date of Event
    April 13, 2011
    Report Date
    April 13, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: FOOT-END COVER SLICED POWER COIL CORD.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PLATE COVER MOVED BECAUSE THE SCREW FROM THE GAS CYLINDER WAS BENT WHICH CAUSED THE POWER COIL CORD TO SPLIT IN HALF. THERE WAS PT INVOLVEMENT. HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1