1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an amber glass bottle; 2. Sonne's…
Recalling firm: Anatox Inc
Elevated lead levels
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 4, 2023.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
1. 030724-1; 030824-2; 030824-3; 040524-1; 040624-2; 051024-1; 051124-2 2. 030924-4; 031024-5; 080824-1
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
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
Original FDA recall reason
Elevated lead levels
Recall details
- Recall number
- F-1005-2023
- Event ID
- 92186
- FDA status
- Terminated
- Initiated
- May 26, 2023
- Reported
- Jul 5, 2023
- Classified
- Jun 23, 2023
- Terminated
- Oct 4, 2023
- Quantity
- 6,777 bottles
- Location
- Richland, MO, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
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
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.