FDA recall record

Ohio Valley Herbal Products Wild'erb Herbal Tea 1.2 oz recall — FDA F-0079-2015

The firm was notified by the Ohio Department of Agriculture that Sassafras Leaves may be an illegal ingredient for their product.

Class IIIclassification
F-0079-2015official record ID
Oct 29, 2014report date

Recall record at a glance

Official recordF-0079-2015
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmOhio Valley Herbal Products, Inc.
Report dateOct 29, 2014
Recall initiation dateNov 20, 2013
Quantity1.2 oz. - 306; 4 oz. - 100
LocationEast Liverpool, OH, United States

Official product description

Wild'erb Herbal Tea 1.2 oz. and 4 oz. paper bags, tea contained less than 5% sassafras leaves.

Why the product was recalled

The firm was notified by the Ohio Department of Agriculture that Sassafras Leaves may be an illegal ingredient for their product.

Distribution information

Product was distributed in CT, IN, MD, OH, PA and WV.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.