BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 2910351 · Received January 4, 2013

    Report

    Report Number
    1831750-2013-90176
    Event Type
    Injury
    Date Received
    January 4, 2013
    Date of Event
    December 7, 2012
    Report Date
    December 7, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION IS ON-GOING; A FOLLOW-UP REPORT WILL BE SUBMITTED WITH RESULTS.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE HI/LO MOTORS WERE STUCK AND STAFF MEMBERS ALLEGEDLY INJURED THEIR BACKS MOVING PTS MORE FREQUENTLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    5298 GOBED II MED/SURG BED A/C HOSPITAL BED FNL STRYKER MEDICAL FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1