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Class II: temporary or reversible health riskTerminated

Oregons Wild Harvest Dried whole elderberry Recall

Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag,…

Oregons Wild Harvest Inc · Redmond, OR

Risk level
Class II
Reported by FDA
May 15, 2019
Recall ID
F-1328-2019
Check your lot numberHow we source this data

Summary

Oregons Wild Harvest recalled Dried whole elderberry starting Apr 26, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1328-2019 on May 15, 2019. Reason: Dried whole Elderberries are recalled due to glass fragments contamination. Status: Terminated.

Why it was recalled

Dried whole Elderberries are recalled due to glass fragments contamination.

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***".

Lot numbers, UPCs & expiration codes

The lot number for 4 oz. bag is 190300173. The lot number for 1 lb. bag is 190300172. There is no best by date or expiration date printed on either product.

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1328-2019
Classification
Class II
Status
Terminated
Recall initiated
Apr 26, 2019
FDA report date
May 15, 2019
Quantity
155/4 oz bags and 197/1 lb bags
Recall type
Voluntary: Firm initiated
Recalling firm
Oregons Wild Harvest Inc

Original FDA data

Every field from FDA enforcement report F-1328-2019, exactly as published.

Show all FDA fields
City
Redmond
State
OR
Status
Terminated
Country
United States
Event ID
82717
Address
1601 NE Hemlock Ave
Code information
The lot number for 4 oz. bag is 190300173. The lot number for 1 lb. bag is 190300172. There is no best by date or expiration date printed on either product.
Postal code
97756-1666
Report date
May 15, 2019
Product type
Food
Recall number
F-1328-2019
Classification
Class II
Recalling firm
Oregons Wild Harvest Inc
Product quantity
155/4 oz bags and 197/1 lb bags
Termination date
Aug 12, 2019
Reason for recall
Dried whole Elderberries are recalled due to glass fragments contamination.
Voluntary / mandated
Voluntary: Firm initiated
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***".
Distribution pattern
CA, FL, GA, HI, ID, IL, MD, ME, MN, NH, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, VT, WA, and WI.
Recall initiation date
Apr 26, 2019
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
May 3, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1328-2019, published May 15, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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