BEUDAMED
    FDA Recall Terminated

    Kendall MONOJECT MAGELLAN SAFETY NEEDLE 21G X 1 inch Product Number: 5551850110

    Recall: Z-0103-05 · Initiated October 8, 2004

    Recall

    Recall Number
    Z-0103-05
    Event Number
    30196
    Firm
    Kendall Healthcare Products Co
    FEI Number
    1282497
    Product Code
    FMI
    Status
    Terminated
    Root Cause
    Other
    Initiated
    October 8, 2004
    Posted
    November 2, 2004
    Terminated
    May 15, 2012
    Address
    15 Hampshire St, Mansfield, MA, 02048-1113

    Description

    Kendall MONOJECT MAGELLAN SAFETY NEEDLE 21G X 1 inch Product Number: 5551850110

    Reason

    Needle cannula may separate from the hub during use

    Action

    Recall letters requesting product return were mailed to all customers on October 8, 2004

    Distribution

    Nationwide