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RECALL RECORD — CLASS IRecall closedF-1523-2013/FDA enforcement
Atlantic Pro Nutrients, INC. Dba Xymogen·Dietary Supplements·May 1, 2013

Xymogen Ep Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy…

What you need to know

Class I

  • What happened

    Undeclared Soy and Milk on the label.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. 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 FDAAK, AL, AR, AZ +36 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameAtlantic Pro Nutrients, INC. Dba Xymogen
Recalling firmAtlantic Pro Nutrients, INC. Dba XymogenOrlando, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • All SKUs
Distribution area
AKALARAZCACOCTDEFLGAIAILINKSKYLAMAMDMEMIMNMOMSNCNJNMNYOHOKPARISCTNTXUTVAWAWIWVWY

AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY, District of Columbia and Hawaii

United States

Quantity affected16, 268 units
Recall initiationFDA report date: June 19, 2013
FDA recall numberF-1523-2013

Beyond the headline

The recall, in context

Atlantic Pro Nutrients, INC. Dba Xymogen initiated this supplements recall on May 1, 2013. The FDA enforcement report states: Undeclared Soy and Milk on the label. The FDA report lists distribution as: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY, District of Columbia and Hawaii.

The FDA enforcement report describes the reason as: Undeclared Soy and Milk on the label.

Xymogen Ep Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy… was made or distributed by Atlantic Pro Nutrients, INC. Dba Xymogen in Orlando, FL, United States. This page reflects FDA report F-1523-2013, dated June 19, 2013.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. 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 has a reasonable probability of causing serious adverse health consequences or death.

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 milk

Symptoms to watch for

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

What to do now

  1. 1Do not eat the product if you have a milk 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 Xymogen Ep Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy… recall?

Atlantic Pro Nutrients, INC. Dba Xymogen recalled Xymogen Ep Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy… in an FDA Class I enforcement action reported as F-1523-2013. Undeclared Soy and Milk on the label.

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 milk 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 Atlantic Pro Nutrients, INC. Dba Xymogen 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-1523-2013. 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

Brand history

More recalls by Atlantic Pro Nutrients, INC. Dba Xymogen

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Class III·

Atlantic Pro Nutrients, INC. Dba Xymogen

Lipichol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription Distributed by: …

Product was labeled as a medical food as opposed to a dietary supplement.

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Class III·

Atlantic Pro Nutrients, INC. Dba Xymogen

Xymogen Lipichol (Omega-3 Phospholipid 540 mg) Medical Food Distributed by Xymogen Orlando, …

Product was labeled as a medical food as opposed to a dietary supplement.

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