BEUDAMED
    FDA Adverse Event Other Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1993071 · Received February 7, 2011

    Report

    Report Number
    1831750-2011-01108
    Event Type
    Other
    Date Received
    February 7, 2011
    Date of Event
    January 10, 2011
    Report Date
    January 10, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: CUSTOMER HAD REMOVED MOTION INTERRUPT PAN WHILE THEY WERE WORKING ON THE BED, THEREBY PREVENTING THE ABILITY TO PROPERLY BURN THE LOWER LIMITS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED WILL RAISE, BUT IT WILL NOT LOWER. THE SERVICE REPORT NOTES DO NOT INDICATE IF THERE WAS PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES 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 MEDICAL 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1