BEUDAMED
    FDA Adverse Event Other Summary report: N

    MODEL 3000 ELECTRIC ACUTE CARE BED

    MDR report key: 470717 · Received July 2, 2003

    Report

    Report Number
    9680128-2003-00006
    Event Type
    Other
    Date Received
    July 2, 2003
    Date of Event
    May 31, 2003
    Report Date
    May 31, 2003
    Manufacturer
    STRYKER BERTEC MEDICAL, INC.
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A PT WAS FOUND ENTRAPPED BETWEEN MATTRESS AND FULL-LENGTH SIDERAIL. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MODEL 3000 ELECTRIC ACUTE CARE BED ELECTRIC HOSPITAL BED FNL STRYKER BERTEC MEDICAL, INC. FLH668NPCM *

    Patients

    Seq Age Sex Outcome Treatment
    1 7 YR Life Threatening MATTRESS BRAND UNK.