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ACTIVE RECALL — CLASS IIActive recallF-1942-2019/FDA enforcement
Nexagen, LLC·Dietary Supplements·May 28, 2019

Acid Rain Ass Kicking Fat Destroyer Apocalypse Labz

What you need to know

Class II

  • What happened

    Product contains insufficient Higenamine and the label incorrectly declares Cayenne Pepper (CapsiMax) and Choline Bitartrate.

  • 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

    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.

Active recall · classified by the FDAAL, FL, GA, NM +2 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameNexagen, LLC
Recalling firmNexagen, LLCFayetteville, GA, United States
UPC / barcodes
6 11138 28792 0
Lot / date codes
  • Lot #9005860 EXP: 1282020
Distribution area
ALFLGANMTNTX

Product was distributed to the following states: AL, FL, GA, NM, TN & TX.

United States

Quantity affected157 bottles/45 capsules
Recall initiationFDA report date: July 31, 2019
FDA recall numberF-1942-2019

Beyond the headline

The recall, in context

Nexagen, LLC initiated this supplements recall on May 28, 2019. The FDA enforcement report states: Product contains insufficient Higenamine and the label incorrectly declares Cayenne Pepper (CapsiMax) and Choline Bitartrate. The FDA report lists distribution as: Product was distributed to the following states: AL, FL, GA, NM, TN & TX.

The FDA enforcement report describes the reason as: Product contains insufficient Higenamine and the label incorrectly declares Cayenne Pepper (CapsiMax) and Choline Bitartrate.

Acid Rain Ass Kicking Fat Destroyer Apocalypse Labz was made or distributed by Nexagen, LLC in Fayetteville, GA, United States. This page reflects FDA report F-1942-2019, dated July 31, 2019.

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 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

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

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 Acid Rain Ass Kicking Fat Destroyer Apocalypse Labz recall?

Nexagen, LLC recalled Acid Rain Ass Kicking Fat Destroyer Apocalypse Labz in an FDA Class II enforcement action reported as F-1942-2019. Product contains insufficient Higenamine and the label incorrectly declares Cayenne Pepper (CapsiMax) and Choline Bitartrate.

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. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Nexagen, LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1942-2019. 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

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