BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MPL TECHNOLOGIES

    MDR report key: 424511 · Received October 23, 2002

    Report

    Report Number
    MW1026535
    Event Type
    Injury
    Date Received
    October 23, 2002
    Report Date
    October 23, 2002
    Manufacturer
    MPL TECHNOLOGIES
    Product Code
    DZM
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    NEEDLE WENT THROUGH CAP. RPTR SUGGESTS THEY DO NOT BUY THIS BRAND OF SYRINGE NEEDLES AGAIN TO PREVENT FURTHER MISHAPS. RPTR FEELS IF ONLY NEEDLE CAP IS MFG A LITTLE THICKER THE NEEDLE WON'T GO THROUGH THE CAP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MPL TECHNOLOGIES NEEDLE HYPODERMIC METAL 27G 1-1/2IN BEVEL-REG DISPO STERILE DZM MPL TECHNOLOGIES H90827 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *