BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VASOVIEW HEMOPRO

    MDR report key: 2210336 · Received August 9, 2011

    Report

    Report Number
    2242352-2011-01172
    Event Type
    Injury
    Date Received
    August 9, 2011
    Report Date
    August 3, 2011
    Manufacturer
    MAQUET CARDIOVASCULAR, LLC
    Product Code
    GEI
    PMA / PMN Number
    K052274
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN ASSISTANT

    Narratives

    Additional Manufacturer Narrative · 1

    H6: THE DEVICE HAS NOT YET BEEN RETURNED TO MAQUET CARDIAC SURGERY FOR INVESTIGATION. WE WILL CONTINUE PURSUING THE DEVICE BEING RETURNED BY THE CUSTOMER. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS RECEIVED. A LOT HISTORY RECORD REVIEW WAS COMPLETED FOR THE REPORTED LOT NUMBER. THERE WERE NO NON CONFORMANCE ISSUE(S) RELATED TO THE DESCRIBED ISSUE. (B)(4).

    Description of Event or Problem · 1

    THE HOSPITAL REPORTED THAT DURING AN ENDOSCOPIC VEIN HARVESTING PROCEDURE, THE HEMOPRO JAW BOOT BROKE OFF. A REPLACEMENT UNIT WAS USED TO COMPLETE THE PROCEDURE. PIECES WERE RETRIEVED THROUGH ORIGINAL INCISION. THE HOSPITAL DID NOT REPORT ANY PATIENT EFFECTS. MAQUET CARDIOVASCULAR ANTICIPATES RETURN OF THE PRODUCT IN QUESTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM GEI MAQUET CARDIOVASCULAR, LLC VH-3000 25035389

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other