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RECALL RECORD — CLASS IIIRecall closedF-1360-2019/FDA enforcement
Barlean's LLC·Food·May 6, 2019

Item Fg 10083, Barlean's, Ultra Dha Fish Oil Omega-3, Lemonade Flavor, 90 Softgels Per Bottle

What you need to know

Class III

  • What happened

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. Fish-derived ingredients were omitted from the label, creating a risk for fish-allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDANationwide (US)More food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameBarlean's LLC
Recalling firmBarlean's LLCFerndale, WA, United States
UPC / barcodes
7 05875 61004 9
Lot / date codes
  • Best By of January 2022 and earlier
Distribution area
Nationwide

nationwide

United States

Quantity affected3 bottles
Recall initiationFDA report date: May 22, 2019
FDA recall numberF-1360-2019

Beyond the headline

The recall, in context

Barlean's LLC initiated this food recall on May 6, 2019. The FDA enforcement report states: Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm. The FDA report lists distribution as: nationwide.

The FDA enforcement report describes the reason as: Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Item Fg 10083, Barlean's, Ultra Dha Fish Oil Omega-3, Lemonade Flavor, 90 Softgels Per Bottle was made or distributed by Barlean's LLC in Ferndale, WA, United States. This page reflects FDA report F-1360-2019, dated May 22, 2019.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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

Undeclared fish

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a fish allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Item Fg 10083, Barlean's, Ultra Dha Fish Oil Omega-3, Lemonade Flavor, 90 Softgels Per Bottle recall?

Barlean's LLC recalled Item Fg 10083, Barlean's, Ultra Dha Fish Oil Omega-3, Lemonade Flavor, 90 Softgels Per Bottle in an FDA Class III enforcement action reported as F-1360-2019. Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Barlean's LLC 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-1360-2019. 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

Brand history

More recalls by Barlean's LLC

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Item Fg 10146, Barlean S, Essential Woman, 120 Count Softgels Per Bottle

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

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