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RECALL RECORD — CLASS IIRecall closedF-1913-2014/FDA enforcement
Nutri-force Nutrition, INC.·Food·Apr 1, 2014

Fish Oil Softgel Capsules in White High Density Poly-ethylene Bottles Labeled in Part: "Major…

What you need to know

Class II

  • What happened

    Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as1000 mg Fish Oil soft gel capsules.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDADistribution not listedMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameNutri-force Nutrition, INC.
Recalling firmNutri-force Nutrition, INC.Miami Lakes, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #107945
Distribution area

The entire lot was sold under two (2) sales orders with the final shipment taking place on 09/25/2013.

United States

Quantity affected9, 456
Recall initiationFDA report date: May 7, 2014
FDA recall numberF-1913-2014

Beyond the headline

The recall, in context

Nutri-force Nutrition, INC. initiated this food recall on April 1, 2014. The FDA enforcement report states: Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as1000 mg Fish Oil soft gel capsules. The FDA report lists distribution as: The entire lot was sold under two (2) sales orders with the final shipment taking place on 09/25/2013.

The FDA enforcement report describes the reason as: Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as1000 mg Fish Oil soft gel capsules.

Fish Oil Softgel Capsules in White High Density Poly-ethylene Bottles Labeled in Part: "Major… was made or distributed by Nutri-force Nutrition, INC. in Miami Lakes, FL, United States. This page reflects FDA report F-1913-2014, dated May 7, 2014.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 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 Fish Oil Softgel Capsules in White High Density Poly-ethylene Bottles Labeled in Part: "Major… recall?

Nutri-force Nutrition, INC. recalled Fish Oil Softgel Capsules in White High Density Poly-ethylene Bottles Labeled in Part: "Major… in an FDA Class II enforcement action reported as F-1913-2014. Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as1000 mg Fish Oil soft gel capsules.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. 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 Nutri-force Nutrition, 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-1913-2014. 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.