Food recall: 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
FDA enforcement event 92186 is a food recall by Anatox Inc of Richland, MO, initiated 26 May 2023 and classified Class III, with 2 product records.
FDA defines Class III as a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences. 13% of the 478 food enforcement events initiated in 2023 carry the same class.
Status: Terminated, terminated 4 Oct 2023. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Anatox Inc.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Anatox Inc, Richland, MO.
Reason for recall
"Elevated lead levels"
Distribution
"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"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1005-2023 | 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 | 6,777 bottles | Class III | Terminated | 5 Jul 2023 |
| F-1006-2023 | Sonne's Detoxificant #7, 1 quart (946 mL) packaged in amber glass bottle. | 2,870 bottles | Class III | Terminated | 5 Jul 2023 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Elevated lead levels"
What does Class III mean?
FDA classifies recalls by relative degree of health hazard. Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
Where was the product distributed?
FDA's distribution pattern field reads: "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"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 4 Oct 2023. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.