BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ABBOTT

    MDR report key: 231276 · Received July 7, 1999

    Report

    Report Number
    MW1016710
    Event Type
    Injury
    Date Received
    July 7, 1999
    Date of Event
    May 8, 1999
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FPA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OR, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    FOLLOWING GENERAL ENDOTRACHEAL ANESTHESIA, PT WAS REPARALYZED DUE TO AN INADVERTENT BOLUS OF NEUROMUSCULAR BLOCK THAT HAD BEEN RETAINED IN THE IV TUBING INJECTION PORT RESERVOIR. MEASUREMENT OF THE RESERVOIR FOLLOWING THIS INCIDENT WAS FOUND TO BE 0.25 - 0.3CC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT NEEDLELESS IV TUBING FPA ABBOTT LABORATORIES, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Life Threatening| R