BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UTERINE MANIPULATOR - 7CM

    MDR report key: 2443682 · Received February 9, 2012

    Report

    Report Number
    3005075853-2012-00539
    Event Type
    Malfunction
    Date Received
    February 9, 2012
    Date of Event
    January 13, 2012
    Report Date
    January 16, 2012
    Manufacturer
    ETHICON ENDO-SURGERY, LLC.
    Product Code
    LKF
    PMA / PMN Number
    K940681
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). DID THE ISSUE OCCUR PRE-OPERATIVE OR INTRA-OPERATIVE? PRE-OPERATIVE. WAS THIS THE INITIAL USE OF THE DEVICE? YES. HOW LONG HAS THE SURGEON BEEN USING THIS DEVICE? NO INFORMATION. WHAT OTHER DEVICES WERE USED IN CONJUNCTION WITH THE DEVICE? NO INFORMATION. WAS THE SALES REP PRESENT DURING THE EVENT? NO.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT DURING A LAPAROSCOPIC OOPHORECTOMY PROCEDURE, THE BALLOON WAS BURST WHEN THE DEVICE WAS CHECKED BEFORE USE FOR THE PATIENT. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UTERINE MANIPULATOR - 7CM LKF ETHICON ENDO-SURGERY, LLC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1