Goldenseal herb c/s, Hydrastis Canadensis, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1388-2019.
Dried spice and herb products potentially contaminated with generic E. coli.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1388-2019.
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 Ameriherb International 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-1388-2019.
AmeriHerb International 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.
Ameriherb International Inc Recall FAQ
Ameriherb International Inc is the subject of a food safety report: Goldenseal herb c/s, Hydrastis Canadensis, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags. The notice was published on April 24, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 36 units are potentially affected.