BEUDAMED
    FDA Recall Terminated

    novaplus, General Purpose Kit, Cat. No. 56603

    Recall: Z-1947-2021 · Initiated May 11, 2021

    Recall

    Recall Number
    Z-1947-2021
    Event Number
    87954
    Firm
    Medical Action Industries, Inc.
    FEI Number
    1030451
    Product Code
    KDD
    Status
    Terminated
    Root Cause
    Process control
    Initiated
    May 11, 2021
    Terminated
    May 10, 2023
    Address
    306 25 Heywood Rd, Arden, NC, 28704-9302

    Description

    novaplus, General Purpose Kit, Cat. No. 56603

    Reason

    There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits

    Action

    Medical Action Industries, Inc. initiated the recall by email on 05/11/2021 Distributors were instructed to notify their customers. The firm is requesting those in possession of the recalled articles discard them.

    Distribution

    US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.

    Quantity

    21 cases of 20 units