BEUDAMED
    FDA Recall Terminated

    Terumo Needle, 30G x 1/2", Product Code NN3013R

    Recall: Z-2006-2019 · Initiated February 8, 2019

    Recall

    Recall Number
    Z-2006-2019
    Event Number
    82212
    Firm
    Terumo Medical Corporation
    FEI Number
    1118880
    Product Code
    FMI
    Status
    Terminated
    Root Cause
    Packaging
    Initiated
    February 8, 2019
    Terminated
    May 8, 2020
    Address
    950 Elkton Blvd, Elkton, MD, 21921-5322

    Description

    Terumo Needle, 30G x 1/2", Product Code NN3013R

    Reason

    There is a potential for a loss of package integrity that may compromise the sterility of the product.

    Action

    Urgent Voluntary Medical Device Recall notification letters dated 2/8/19 were sent to customers.

    Distribution

    The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

    Quantity

    81,000