BEUDAMED
    FDA Recall Terminated

    Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS

    Recall: Z-1818-2019 · Initiated April 23, 2019

    Recall

    Recall Number
    Z-1818-2019
    Event Number
    82865
    Firm
    Arrow International Inc
    FEI Number
    3015859709
    Product Code
    PND
    Status
    Terminated
    Root Cause
    Process control
    Initiated
    April 23, 2019
    Terminated
    January 13, 2021
    Address
    2400 Bernville Rd, Reading, PA, 19605-9607

    Description

    Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS

    Reason

    Lidstock states the incorrect expiration date for the product

    Action

    Arrow International initiated recall by letter dated April 23,2019 described the problem, health risk and action to take: If you have affected stock in inventory, immediately discontinue use and quarantine the products. 2. Complete the enclosed Acknowledgement Form indicating whether you do or do not have stock and fax it to 1-855-419-8507 or email to [email protected]. A customer service representative will contact you with a Return Goods Authorization (RGA) number and provide instructions for the return of products. Distributors requested to subrecall. Questions, contact your local sales representative or Customer Service at 1-866-396-2111.

    Distribution

    Nationwide Foreign:

    Quantity

    430 units