BEUDAMED
    FDA Recall Terminated

    First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B

    Recall: Z-3046-2020 · Initiated August 18, 2020

    Recall

    Recall Number
    Z-3046-2020
    Event Number
    86335
    Firm
    Ameditech Inc
    FEI Number
    3003789989
    Product Code
    DKC
    Status
    Terminated
    Root Cause
    Process control
    Initiated
    August 18, 2020
    Terminated
    September 30, 2024
    Address
    9940 Mesa Rim Rd, San Diego, CA, 92121-2910

    Description

    First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B

    Reason

    Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.

    Action

    A Field Corrective Action Notice letter was sent to affected consignees. The Customer notifications commenced on 19-Aug-2020. The consignees are requested to return all non-expired product in their possession to the recalling firm. Method of Notification, 1st contact: Written field corrective action notification letters will be sent via certified mail with delivery tracking to each consignee along with a pre-paid return label to return any product remaining in stock. 2nd & 3rd contact: Telephone, follow up email, or written mail communication will be used as necessary.

    Distribution

    US - Nationwide OUS - Australia, France, Germany, New Zealand, Singapore and Spain

    Quantity

    2,555,630 units