BEUDAMED
    FDA Recall Terminated

    3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

    Recall: Z-2007-2019 · Initiated February 1, 2019

    Recall

    Recall Number
    Z-2007-2019
    Event Number
    82138
    Firm
    Becton Dickinson & Company
    FEI Number
    2243072
    Product Code
    FMF
    Status
    Terminated
    Root Cause
    Under Investigation by firm
    Initiated
    February 1, 2019
    Terminated
    June 11, 2020
    Address
    1 Becton Dr, Franklin Lakes, NJ, 07417-1815

    Description

    3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

    Reason

    The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.

    Action

    Urgent Medical Device Recall notification letters dated 2/1/19 were sent to customers.

    Distribution

    The products were distributed to the following US states: FL, IL, KS, MA, ND, NH, NY, OH, PA, RI, SC, VA, and WI. The products were distributed to the following foreign countries: Suriname.

    Quantity

    460,800