FDA recall record

AmeriHerb International Goldenseal herb c/s, Hydrastis Canadensis, Not for use during recall — FDA F-1388-2019

Dried spice and herb products potentially contaminated with generic E. coli.

Class IIclassification
F-1388-2019official record ID
May 22, 2019report date

Recall record at a glance

Official recordF-1388-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAmeriHerb International Inc.
Report dateMay 22, 2019
Recall initiation dateApr 24, 2019
Quantity36 lbs
LocationAmes, IA, United States

Official product description

Goldenseal herb c/s, Hydrastis Canadensis, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags

Why the product was recalled

Dried spice and herb products potentially contaminated with generic E. coli.

Distribution information

Customers nationwide (including Puerto Rico). Foreign distribution to Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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