BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HUDSON INCENTIVE SPIROMETER, INTL

    MDR report key: 2447265 · Received January 30, 2012

    Report

    Report Number
    3004365956-2012-00032
    Event Type
    Malfunction
    Date Received
    January 30, 2012
    Report Date
    January 16, 2012
    Manufacturer
    TELEFLEX MEDICAL
    Product Code
    BWF
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE SAMPLE WAS NOT RECEIVED BY THE MANUFACTURER AT THE TIME OF THIS REPORT. A FOLLOW-UP REPORT WILL BE SENT WHEN COMPLETION OF INVESTIGATION.

    Description of Event or Problem · 1

    THE EVENT IS REPORTED AS: "COMPLAINT ALLEGES THAT CRACKS WERE FOUND AT THE MOUTHPIECES. THE ALLEGED DEFECT WAS DISCOVERED DURING INCOMING INSPECTION." NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HUDSON INCENTIVE SPIROMETER, INTL SPIROMETER BWF TELEFLEX MEDICAL 02G1002425

    Patients

    Seq Age Sex Outcome Treatment
    1