Sonne's Detoxificant #7
Reason Elevated lead levels
1. VIT-RA-TOX Calphonite #38 recall
Recalled by Anatox Inc · Richland, MO, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Elevated lead levels
Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.
What was recalled
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
Quantity: 6,777 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
1. 030724-1; 030824-2; 030824-3; 040524-1; 040624-2; 051024-1; 051124-2 2. 030924-4; 031024-5; 080824-1
Where it was sold
Alabama Arizona California Colorado Connecticut Florida Georgia Illinois Indiana Kansas Kentucky Massachusetts Maryland Minnesota Missouri North Carolina New Mexico New York Ohio Oregon Pennsylvania Tennessee Texas Utah Virginia Vermont Wisconsin
FDA's distribution note: 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
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Anatox Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 26, 2023
- In FDA report of
- Jul 5, 2023
- Terminated
- Oct 4, 2023
- FDA recall number
- F-1005-2023 · event 92186
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.