BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE ACUTE CARE BED 3/01

    MDR report key: 1903325 · Received November 12, 2010

    Report

    Report Number
    1831750-2010-03773
    Event Type
    Malfunction
    Date Received
    November 12, 2010
    Date of Event
    October 15, 2010
    Report Date
    October 15, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: FOOT BOARD COMPONENTS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE FOOTBOARD IS BROKEN. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE WAS PT INVOLVEMENT OR IF THERE WAS ADVERSE CONSEQUENCES TO REPORT.

    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 CORP., MEDICAL DIV. 3000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK