BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2183157-1999-00323

    MDR report key: 257258 · Received December 30, 1999

    Report

    Report Number
    2183157-1999-00323
    Event Type
    Malfunction
    Date Received
    December 30, 1999
    Date of Event
    December 2, 1999
    Report Date
    December 29, 1999
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    NELLCOR PURITAN BENNETT RECEIVED A CALL FROM A REPRESENTATIVE ON 12/02/1999. REPRESENTATIVE CALLED TO REPORT THE FOLLOWING PROBLEM: UNIT WILL NOT CYCLE.

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other