BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 2221733 · Received August 15, 2011

    Report

    Report Number
    1831750-2011-08648
    Event Type
    Malfunction
    Date Received
    August 15, 2011
    Date of Event
    July 18, 2011
    Report Date
    July 18, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: FOWLER SUPPORT, FOOTBOARD. CONCLUSION: CUSTOMER HAS RECEIVED THE ESTIMATE FOR THE POST TO REPAIR THE BED AND HAS NOT DECIDE TO COMPLETE REPAIRS AT THIS TIME.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE FOWLER SUPPORT WAS BENT AND THE BED COULD NOT REACH THE LOWEST HEIGHT, THE FOWLER LIMIT CARD WAS MISSING, THE FOOT END POWER CABLE WAS MISSING CAUSING THE FOOT END LIFT TO BE INOPERABLE, THERE WAS AN ERROR ON THE FOOTBOARD CAUSING THE FOOTBOARD TO NOT OPERATE PROPERLY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCE ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1