RECALL RECORD — CLASS IIRecall closedF-0709-2025/FDA enforcement

Fresh Flax Oil Omega 3-6-9 Organic Flaxseed Oil 16 FL OZ / 473 ML, Dietary Supplement, Black…

What you need to know

Class II
  • What happened

    Undeclared allergens: Soy lecithin

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • 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 FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameBioriginal Food & Science Corporation
Recalling firmBioriginal Food & Science CorporationSaskatoon, Canada
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot Code: PRP403337
Distribution area

Puerto Rico

Puerto Rico

Quantity affected61 bottles
Recall initiationFDA report date: April 9, 2025
FDA recall numberF-0709-2025

Beyond the headline

The recall, in context

Bioriginal Food & Science Corporation initiated this supplements recall on March 21, 2025. The FDA enforcement report states: Undeclared allergens: Soy lecithin. The FDA report lists distribution as: Puerto Rico.

The FDA enforcement report describes the reason as: Undeclared allergens: Soy lecithin

Fresh Flax Oil Omega 3-6-9 Organic Flaxseed Oil 16 FL OZ / 473 ML, Dietary Supplement, Black… was made or distributed by Bioriginal Food & Science Corporation in Saskatoon, Canada. This page reflects FDA report F-0709-2025, dated April 9, 2025.

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, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

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 lot and date codes 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 soy

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a soy 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 soy allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a soy 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 Fresh Flax Oil Omega 3-6-9 Organic Flaxseed Oil 16 FL OZ / 473 ML, Dietary Supplement, Black… recall?

Bioriginal Food & Science Corporation recalled Fresh Flax Oil Omega 3-6-9 Organic Flaxseed Oil 16 FL OZ / 473 ML, Dietary Supplement, Black… in an FDA Class II enforcement action reported as F-0709-2025. Undeclared allergens: Soy lecithin

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. Do not eat the product if you have a soy 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 Bioriginal Food & Science Corporation 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-0709-2025. 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

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