BEUDAMED
    FDA Adverse Event Summary report: N

    GOBED II MED/SURG

    MDR report key: 1953464 · Received December 28, 2010

    Report

    Report Number
    9680128-2010-05261
    Date Received
    December 28, 2010
    Date of Event
    November 30, 2010
    Report Date
    November 30, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE NURSE CALL AND BED EXIT ARE CONSTANTLY ALARMING. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II MED/SURG A/C HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK