BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEDTRONIC/COVIDIEN SURGICAL STAPLERS

    MDR report key: 20639651 · Received November 7, 2024

    Report

    Report Number
    MW5162323
    Event Type
    Other
    Date Received
    November 7, 2024
    Date of Event
    November 17, 2021
    Report Date
    November 5, 2024
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    GAG
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    ATTORNEY
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MS. (B)(6). SUFFERED SERIOUS INJURY REQUIRING SURGICAL INTERVENTION USING AN FDA GRADING OF INJURIES RESULTING FROM USE OF A MALFUNCTIONING MEDTRONIC/COVIDIEN SURGICAL STAPLER. HER INJURIES WHICH WERE CAUSED BY AN ANASTOMOTIC LEAK WITHIN 6 DAYS OF SURGERY INCLUDE: LIFE THREATENING INJURIES (INTENSIVE CARE TREATMENT, ACUTE KIDNEY INJURY, SEPSIS, EXTENDED HOSPITALIZATION, AND SUBSEQUENT SURGERIES) TO CORRECT ANY INJURIES. REF REPORTS: MW5162319, MW5162320, MW5162321, MW5162322.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1540475 MEDTRONIC/COVIDIEN SURGICAL STAPLERS STAPLER, SURGICAL GAG MEDTRONIC, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown