BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    B-D

    MDR report key: 1338200 · Received March 5, 2009

    Report

    Report Number
    MW5010216
    Event Type
    Malfunction
    Date Received
    March 5, 2009
    Date of Event
    October 1, 2008
    Report Date
    March 5, 2009
    Manufacturer
    B-D
    Product Code
    KYX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    B-D 3 ML ORAL SYRINGE OBTAINED AS A REPLACEMENT FOR BAXA 3 ML ORAL SYRINGE DUE TO LATTER BEING ON BACK ORDER. INK ON BARREL IS EASILY RUBBED OFF BY FINGERS. GRADUATIONS IN 0.2 ML INSTEAD OF 0.1 ML. SYRINGE WAS ORDERED FOR PEDIATRIC ACUTE CARE/REHAB HOSPITAL. ORAL SYRINGE NOT USED - RETURNED TO DISTRIBUTOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 B-D ORAL SYRINGE - 3 ML KYX B-D

    Patients

    Seq Age Sex Outcome Treatment
    1