BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE ACUTE CARE BED 3/01

    MDR report key: 2022160 · Received March 10, 2011

    Report

    Report Number
    1831750-2011-02348
    Event Type
    Malfunction
    Date Received
    March 10, 2011
    Date of Event
    February 28, 2011
    Report Date
    February 28, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END OF THE BED COULD NOT BE LOWERED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE ACUTE CARE BED 3/01 A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1