Food recall

Anatox Inc recall: 1

Anatox Inc, of Richland, MO, recalled 1 and 1 other product. The FDA's reason: “Elevated lead levels.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on May 26, 2023, and the FDA first listed it in its Enforcement Report of July 5, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class III

It is unlikely to cause harm

Why

Lead or other chemicals

Status

Terminated

Closed October 4, 2023

The recall

Company
Anatox Inc (Richland, MO)
Reason, in FDA's words
“Elevated lead levels”
Where it was sold
Distributors, retailers, and consumers in AL, AZ, CA, CT, CO, FL, GA, IL, IN, KS, KY, MA, MD, MN, MO, NC, NM, NY, OH, OR, PA, TN, TX, UT, VA, VT, WI
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
92186

The 2 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-1005-2023 Class III

    1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an amber glass bottle; 2. Sonne's Calphonite #2, 15 Fl. oz. (444 ml) in an amber glass bottle

    Codes: 1. 030724-1; 030824-2; 030824-3; 040524-1; 040624-2; 051024-1; 051124-2 2. 030924-4; 031024-5; 080824-1

    Quantity: 6,777 bottles

  • F-1006-2023 Class III

    Sonne's Detoxificant #7, 1 quart (946 mL) packaged in amber glass bottle.

    Codes: 021424-1, 021724-4

    Quantity: 2,870 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 5, 2023.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.