BEUDAMED
    FDA Recall Open, Classified

    Alinity m System, Part No. 08N53-002

    Recall: Z-0460-2022 · Initiated December 6, 2021

    Recall

    Recall Number
    Z-0460-2022
    Event Number
    89166
    Firm
    Abbott Molecular, Inc.
    FEI Number
    3005248192
    Product Code
    MZP
    Status
    Open, Classified
    Root Cause
    Under Investigation by firm
    Initiated
    December 6, 2021
    Address
    1300 E Touhy Ave, Des Plaines, IL, 60018-3315

    Description

    Alinity m System, Part No. 08N53-002

    Reason

    There is a potential for abnormal (non-sigmoidal) amplification curves.

    Action

    On December 06, 2021 Abbott Molecular issued a Product Correction letter to all customers who received an Alinity m instrument (List Number 08N53 002). Customers are instructed to follow the Necessary Actions outlined in the Customer Letter until an Abbott Molecular representative adjusts the customers clamp bar. Abbott personnel will follow up with customers by e mailing and or follow up visits/phone calls.

    Distribution

    Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Brazil, Cambodia, Canada, Chile, Colombia, Czech Republic, Egypt, El Salvador, Estonia, Finland, France, Germany, Hong Kong, Ireland, Israel, Italy, Japan, Malawi, Malaysia, Mexico, Montenegro, Morocco, Mozambique, Netherlands, New Zealand, Norway, Pakistan, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Uganda, United Kingdom, and Vietnam.

    Quantity

    742 devices