BEUDAMED
    FDA Adverse Event Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 2012725 · Received February 28, 2011

    Report

    Report Number
    1831750-2011-01956
    Date Received
    February 28, 2011
    Date of Event
    February 7, 2011
    Report Date
    February 7, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT/CONCLUSION: THE POWER CORD WAS FOUND TO NOT BE FULLY SECURED IN THE BED RECEPTACLE. THE SERVICE TECH RE-ESTABLISHED THE CONNECTION AND POWER WAS RESTORED TO THE UNIT.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAS NO POWER. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1