VerifyRecall
Alerts
RECALL RECORD — CLASS IIRecall closedF-1328-2019/FDA enforcement
Oregons Wild Harvest INC·Dietary Supplements·Apr 26, 2019

Dried Whole Elderberry, Oregon S Wild Harvest Brand, Packaged in Metalized Plastic Bag, NET WT

What you need to know

Class II

  • What happened

    Dried whole Elderberries are recalled due to glass fragments contamination.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Glass fragments can cause cuts, choking or internal injury if swallowed.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDACA, FL, GA, HI +19 moreMore supplements

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Share via WhatsApp

Match before you discard

Product identification

Source: FDA FOOD

Brand nameOregons Wild Harvest INC
Recalling firmOregons Wild Harvest INCRedmond, OR, United States
UPC / barcodes
7 06195 05352 37 06195 01352 7
Lot / date 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.
Distribution area
CAFLGAHIIDILMDMEMNNHNJNVNYOHORPASCTNTXUTVTWAWI

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

United States

Quantity affected155/4 oz bags and 197/1 lb bags
Recall initiationFDA report date: May 15, 2019
FDA recall numberF-1328-2019

Beyond the headline

The recall, in context

Oregons Wild Harvest INC initiated this supplements recall on April 26, 2019. The FDA enforcement report states: Dried whole Elderberries are recalled due to glass fragments contamination. The FDA report lists distribution as: CA, FL, GA, HI, ID, IL, MD, ME, MN, NH, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, VT, WA, and WI.

The FDA enforcement report describes the reason as: Dried whole Elderberries are recalled due to glass fragments contamination.

Dried Whole Elderberry, Oregon S Wild Harvest Brand, Packaged in Metalized Plastic Bag, NET WT was made or distributed by Oregons Wild Harvest INC in Redmond, OR, United States. This page reflects FDA report F-1328-2019, dated May 15, 2019.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, glass fragments can cause cuts, choking or internal injury if swallowed.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Glass contamination

Possible health effects

Glass fragments can cause cuts to the mouth, throat or digestive tract. Do not inspect or taste a suspect product.

Higher-risk groups

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk of injury.

What to do now

  1. 1Stop eating or using the product and do not attempt to remove fragments by tasting it.
  2. 2Seek medical care if anyone has swallowed glass, has throat or abdominal pain, or is vomiting blood.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund; follow the recall notice for disposal.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Dried Whole Elderberry, Oregon S Wild Harvest Brand, Packaged in Metalized Plastic Bag, NET WT recall?

Oregons Wild Harvest INC recalled Dried Whole Elderberry, Oregon S Wild Harvest Brand, Packaged in Metalized Plastic Bag, NET WT in an FDA Class II enforcement action reported as F-1328-2019. Dried whole Elderberries are recalled due to glass fragments contamination.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop eating or using the product and do not attempt to remove fragments by tasting it. Seek medical care if anyone has swallowed glass, has throat or abdominal pain, or is vomiting blood. Keep the packaging and contact the retailer or manufacturer about a refund; follow the recall notice for disposal.

Is the Oregons Wild Harvest INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1328-2019. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Related alerts

Recent Glass recalls

All alerts
Class II·

Gearharts Fine Chocolates, INC.

Gearharts Fine Chocolates NET WT

Foreign Object - Broken glass was found in a piece of finished product.

CA, CT, GA +14 moreFood
Class II·

Dreyer's Grand Ice Cream INC.

Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 Ounce, with

Foreign object: products may contain glass pieces

AL, AR, AZ +30 moreFood

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.