BEUDAMED
    FDA Adverse Event Other Summary report: N

    SAGE PRODUCTS

    MDR report key: 35863 · Received August 14, 1996

    Report

    Report Number
    1419181-1996-00042
    Event Type
    Other
    Date Received
    August 14, 1996
    Date of Event
    May 23, 1996
    Report Date
    August 14, 1996
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A RN WAS GOING TO FINAL DISPOSE OF A FULL SHARPS CONTAINER AND AS SHE REACHED HER HAND AROUND THE CONTAINER TO PICK IT UP, SHE REPORTEDLY RECEIVED A NEEDLESTICK FROM A NEEDLE ATTACHED TO A 3CC SYRINGE THAT HAD PROTRUDED THROUGH THE SIDE OF THE CONTAINER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SAGE PRODUCTS SHARPS DISPOSABLE CONTAINER MMK SAGE PRODUCTS, INC. 8900 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN