BEUDAMED
    FDA Recall Open, Classified

    Diasol Acid Concentrate REF G100325-10Dex 100

    Recall: Z-0207-2025 · Initiated July 27, 2022

    Recall

    Recall Number
    Z-0207-2025
    Event Number
    95334
    Firm
    Diasol, Inc
    FEI Number
    3007137482
    Product Code
    KPO
    Status
    Open, Classified
    Root Cause
    Labeling mix-ups
    Initiated
    July 27, 2022
    Posted
    October 23, 2024
    Address
    310 S 43rd Ave, Ste B, Phoenix, AZ, 85009-4606

    Description

    Diasol Acid Concentrate REF G100325-10Dex 100

    Reason

    Due to labeling issue. The box label is different that the gallon label in that gallon label shows a lower Calcium concentration than the box label.

    Action

    On 07/26/2022, the firm communicated via email with customer that 2 case were incorrectly labeled. Cases marked 3K 2.5ca have inside box label as 3K 2.0ca. Customer was instructed not to use the product and the firm picked up mislabeled product.

    Distribution

    U.S. Nationwide distribution in the state of AZ.

    Quantity

    852 gallon bottles