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RECALL RECORD — CLASS IIRecall closedF-1926-2013/FDA enforcement
Healthmaxx Global INC.·Dietary Supplements·Jun 10, 2013

Hyper Ii Dha/epa, 100 Count Softgels

What you need to know

Class II

  • What happened

    In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Fish-derived ingredients were omitted from the label, creating a risk for fish-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 FDACA, MD, NYMore supplements

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Product identification

Source: FDA FOOD

Brand nameHealthmaxx Global INC.
Recalling firmHealthmaxx Global INC.Hacienda Heights, CA, United States
UPC / barcodes
6 65176 05274 3
Lot / date codes
  • Lot # F0202 UPC 6 65176 05274 3
Distribution area
CAMDNY

CA, MD, and NY

United States

Quantity affected2863 bottles
Recall initiationFDA report date: October 2, 2013
FDA recall numberF-1926-2013

Beyond the headline

The recall, in context

Healthmaxx Global INC. initiated this supplements recall on June 10, 2013. The FDA enforcement report states: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained. The FDA report lists distribution as: CA, MD, and NY.

The FDA enforcement report describes the reason as: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.

Hyper Ii Dha/epa, 100 Count Softgels was made or distributed by Healthmaxx Global INC. in Hacienda Heights, CA, United States. This page reflects FDA report F-1926-2013, dated October 2, 2013.

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 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 Hyper Ii Dha/epa, 100 Count Softgels recall?

Healthmaxx Global INC. recalled Hyper Ii Dha/epa, 100 Count Softgels in an FDA Class II enforcement action reported as F-1926-2013. In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the…

What are the symptoms of Undeclared fish exposure?

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

How quickly can Undeclared fish symptoms appear?

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

Who is most at risk from Undeclared fish?

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

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 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.

How do I get a refund from Healthmaxx Global INC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1926-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Healthmaxx Global 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-1926-2013. 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.