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Oregons Wild Harvest Inc Recall: Dried whole Elderberries are recalled due to glass fragments contamination.

United States

TerminatedClass II

Company
Oregons Wild Harvest Inc
Product
Dried whole elderberry, Oregon s Wild Harvest brand, package…
Recall date
April 26, 2019
Terminated
August 12, 2019
Source
FDA

Reason for recall

Dried whole Elderberries are recalled due to glass fragments contamination.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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***". Not published in this source record 155/4 oz bags and 197/1 lb bags 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.

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1328-2019
Event ID
82717
Status
Terminated
Classification
Class II
Company
Oregons Wild Harvest Inc
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***".
Quantity
155/4 oz bags and 197/1 lb bags
Reason
Dried whole Elderberries are recalled due to glass fragments contamination.
Recall initiation date
April 26, 2019
Report date
May 15, 2019
Classification date
Not published in this source record
Termination date
August 12, 2019
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.
UPC, lot, and 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.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Oregons Wild Harvest Inc

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Florida 1
Georgia 1
Hawaii 1
Idaho 1
Illinois 1
Maryland 1
Maine 1
Minnesota 1
New Hampshire 1
New Jersey 1
Nevada 1
New York 1
Ohio 1
Oregon 1
Pennsylvania 1
South Carolina 1
Tennessee 1
Texas 1
Utah 1
Vermont 1
Washington 1
Wisconsin 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.