BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8020889-1999-00028

    MDR report key: 257038 · Received December 22, 1999

    Report

    Report Number
    8020889-1999-00028
    Event Type
    Malfunction
    Date Received
    December 22, 1999
    Date of Event
    December 6, 1999
    Report Date
    December 6, 1999
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    TUBE COLLAPSED IN MULTIPLE SPOTS.

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN