BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DOBHOFF

    MDR report key: 7006596 · Received November 7, 2017

    Report

    Report Number
    MW5073166
    Event Type
    Injury
    Date Received
    November 7, 2017
    Date of Event
    October 14, 2017
    Report Date
    November 3, 2017
    Manufacturer
    UNK
    Product Code
    BSS
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2017 AS DOBHOFF TUBE REMOVED, MD, RN AND PT HEARD POP AND DOBHOFF TUBE REMOVED AND DID NOT HAVE WEIGHTED TIP PRESENT ON END OF TUBE. ABD XRAY SHOWED NO TIP. ON (B)(6) 2017 SINUS XRAY SHOWED TIP IN R NARE. ENT CONSULTED AND REMOVED AT BEDSIDE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    785508 DOBHOFF NASALGASTRIC TUBE BSS UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 20 YR Required Intervention