BEUDAMED
    FDA Adverse Event Other Summary report: N

    BLOOD/FLUID WARMER

    MDR report key: 2217386 · Received July 15, 2011

    Report

    Report Number
    1313850-2011-00169
    Event Type
    Other
    Date Received
    July 15, 2011
    Date of Event
    June 15, 2011
    Report Date
    June 15, 2011
    Manufacturer
    STRYKER CORP DBA GAYMAR
    Product Code
    LGZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE UNIT HAD BEEN DROPPED; THE HOUSING WAS DAMAGED AND THERE WERE EXPOSED ELECTRICAL COMPONENTS. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BLOOD/FLUID WARMER FUILD WARMER LGZ STRYKER CORP DBA GAYMAR FW600 NA

    Patients

    Seq Age Sex Outcome Treatment
    1