BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ENDOPATH CLAW EXTRACTOR

    MDR report key: 149672 · Received February 16, 1998

    Report

    Report Number
    1527736-1998-00382
    Event Type
    Malfunction
    Date Received
    February 16, 1998
    Date of Event
    January 14, 1998
    Report Date
    January 19, 1998
    Manufacturer
    SYMBIOSIS CORP.
    Product Code
    KNS
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SENT 04/13/1999. H10: MEDWATCH CREATED IN ERROR.

    Description of Event or Problem · 1

    IT WAS REPORTED DURING A LAPAROSCOPIC CHOLECYSTECTOMY WHILE USING THE DEX41 THE JAWS OF THE GRASPER BROKE APART. THERE WAS NO CONSEQUENCE TO THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENDOPATH CLAW EXTRACTOR EXTRACTOR KNS SYMBIOSIS CORP. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other