BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE ACUTE CARE BED

    MDR report key: 2023939 · Received February 14, 2011

    Report

    Report Number
    1831750-2011-01371
    Event Type
    Malfunction
    Date Received
    February 14, 2011
    Date of Event
    January 21, 2011
    Report Date
    January 21, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS - GROUND PRONG.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE GROUND PRONG IS BROKEN OFF POWER CORD. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1