BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MPS DELIVERY SET

    MDR report key: 5138710 · Received October 8, 2015

    Report

    Report Number
    1649914-2015-00071
    Event Type
    Injury
    Date Received
    October 8, 2015
    Date of Event
    September 10, 2015
    Report Date
    September 10, 2015
    Manufacturer
    QUEST MEDICAL, INC.
    Product Code
    DTR
    PMA / PMN Number
    K953838
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO PRODUCT SAMPLE WAS RETURNED FOR ANALYSIS AND NO LOT NUMBER WAS PROVIDED. QUEST MEDICAL, INC. HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. QUEST MEDICAL, INC. DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    THE HOSPITAL PERFUSIONIST REPORTED AN ISSUE ENCOUNTERED WITH THE MPS DELIVERY SET DURING USE. HE STATED ONLY THAT THE DELIVERY SET RUPTURED DURING USE, AT THE END OF THE PROCEDURE WHILE WARMING. HE ORIGINALLY STATED THE DEVICE WOULD BE RETURNED FOR ANALYSIS; HOWEVER, MULTIPLE ATTEMPTS TO OBTAIN THE SAMPLE FROM THE HOSPITAL WERE UNSUCCESSFUL. THE LOT NUMBER WAS NOT PROVIDED. THE APPROXIMATE VOLUME OF BLOOD LOSS WAS NOT PROVIDED. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THE ALLEGED EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    667379 MPS DELIVERY SET CPBP HEAT EXCHANGER DTR QUEST MEDICAL, INC. 5001102

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention