BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AUTO SUTURE MULTIFIRE ENDO GIA 30-3.5

    MDR report key: 92194 · Received May 16, 1997

    Report

    Report Number
    2647580-1997-00510
    Event Type
    Malfunction
    Date Received
    May 16, 1997
    Date of Event
    April 17, 1997
    Report Date
    April 18, 1997
    Manufacturer
    UNITED STATES SURGICAL CORP
    Product Code
    GCJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    6/23/1997-SUPPLEMENTAL REPORT #1 SUBMITTED TO FDA.

    Description of Event or Problem · 1

    DURING AN ATYPICAL SEGMENTIAL RESECTION PROCEDURE, THE KNIFE DID NOT CUT. THE SURGEON APPLIED ANOTHER DEVICE WITHOUT PT INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AUTO SUTURE MULTIFIRE ENDO GIA 30-3.5 DISPOSABLE SURGICAL STAPLER GCJ UNITED STATES SURGICAL CORP NA P7A172

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN