Sonne's Detoxificant #7, 1 quart (946 mL) packaged in amber glass bottle.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1006-2023.
Elevated lead levels
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1006-2023.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Anatox Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1006-2023.
Anatox Inc
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Anatox Inc Recall FAQ
Anatox Inc is the subject of a food safety report: Sonne's Detoxificant #7, 1 quart (946 mL) packaged in amber glass bottle.. The notice was published on May 26, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 2,870 units are potentially affected.