BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EZ-PRO R4 AMBUL COT

    MDR report key: 1920537 · Received December 7, 2010

    Report

    Report Number
    1831750-2010-04594
    Event Type
    Injury
    Date Received
    December 7, 2010
    Date of Event
    November 4, 2010
    Report Date
    November 4, 2010
    Manufacturer
    STRYKER CORP. MEDICAL DIV.
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    COT DROP.

    Description of Event or Problem · 1

    I WAS REPORTED THAT ALLEGEDLY THE COT DROPPED AND A PATIENT WAS INJURED. UPON FURTHER INVESTIGATION IT WAS REPORTED BY THE EMT'S THAT NO VISUAL INJURIES WERE NOTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EZ-PRO R4 AMBUL COT STRETCHER, WHEELED FPO STRYKER CORP. MEDICAL DIV. 6092 NA

    Patients

    Seq Age Sex Outcome Treatment
    1