FDA recall record

Oregons Wild Harvest Dried whole elderberry, Oregon s Wild Harvest brand, packaged recall — FDA F-1328-2019

Dried whole Elderberries are recalled due to glass fragments contamination.

Class IIclassification
F-1328-2019official record ID
May 15, 2019report date

Recall record at a glance

Official recordF-1328-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmOregons Wild Harvest Inc.
Report dateMay 15, 2019
Recall initiation dateApr 26, 2019
Quantity155/4 oz bags and 197/1 lb bags
LocationRedmond, OR, United States

Official product description

Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag, net wt. 4 oz or 1 lb. Each case contains 12 bags. Item # for 4 oz. is 15352. UPC of 4 oz. bag is 7 06195 05352 3. Item # for 1 lb. is 11352. UPC of 1 lb. bag is 7 06195 01352 7. The label is read in part: "***Elderberry Whole *** Herbal Supplement ***Ingredients: Organic Elderberry (Sambucus sp.) *** Suggested Use: Crush or grind berry. Add 1 teaspoon to a cup of boiling water. Steep for 5 minutes, strain and enjoy hot or cold daily*** Oregon s Wild Harvest 1601 NE Hemlock Avenue, Redmond, OR 97756***".

Why the product was recalled

Dried whole Elderberries are recalled due to glass fragments contamination.

Distribution information

CA, FL, GA, HI, ID, IL, MD, ME, MN, NH, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, VT, WA, and WI.

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: 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

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