Use caution Food recall · FDA · Published May 28, 2019

Nexagen Recalls Acid Rain Dietary Supplement Due to Labeling Errors

Nexagen recalls 157 bottles of Acid Rain dietary supplement. The product contains insufficient Higenamine and mislabels ingredients like Cayenne Pepper.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #F-1942-2019Food Nexagen ›

Use caution until it’s fixed

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

Take action

Contact the company

Recalling firmNexagen, LLC630 Highway 314 Ste 1011 · Fayetteville, GA 30214-7917

✎ GovInfoNow plain-language explainer

Nexagen, LLC is recalling one lot of its 'Acid Rain Ass Kicking Fat Destroyer Apocalypse Labz' dietary supplement because the label does not accurately reflect the contents. Specifically, the product contains less Higenamine than stated and incorrectly lists Cayenne Pepper (CapsiMax) and Choline Bitartrate as ingredients. This recall affects 157 bottles distributed in Alabama, Florida, Georgia, New Mexico, Tennessee, and Texas. Read more at govinfonow.com/recall/17416-nexagen-recalls-acid-rain-dietary-supplement-due-to-labeling-errors.

Source Summary by GovInfoNow · govinfonow.com/recall/17416-nexagen-recalls-acid-rain-dietary-supplement-due-to-labeling-errors · Updated October 11, 2026 · FDA enforcement record: FDA #F-1942-2019

Cite this page

“Nexagen Recalls Acid Rain Dietary Supplement Due to Labeling Errors.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/17416-nexagen-recalls-acid-rain-dietary-supplement-due-to-labeling-errors. Based on FDA recall #F-1942-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1942-2019%22&limit=1).

Nexagen, LLC voluntarily recalled one dietary supplement containing insufficient Higenamine and incorrectly declared ingredients, according to the FDA on May 28, 2019. The Food and Drug Administration announced the Class II recall of Acid Rain Fat Destroyer Supplement products distributed in six states.

How to tell if you have it

Brand: Nexagen
Product: ACID RAIN ASS KICKING FAT DESTROYER APOCALYPSE LABZ; 45 CAPSULES; 1 DIETARY SUPPLEMENT
UPC: 6 11138 28792 0
Lot #: 9005860
Distribution states: AL, FL, GA, NM, TN & TX

The hazard

The product contains insufficient Higenamine and the label incorrectly declares Cayenne Pepper (CapsiMax) and Choline Bitartrate. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Avion Prenate Chewable Prenatal Vitamin Recall (2025-10-29), Shaman Botanicals Recalls White Vein Chewable Tablets Due to Dosage Error (2026-02-13), and Sinus Cap Herbal Supplement Recall (2025-11-20).

How to tell if you have this one

Check your bottle for the product name 'ACID RAIN ASS KICKING FAT DESTROYER APOCALYPSE LABZ' containing 45 capsules. Verify the UPC is 6 11138 28792 0 and the Lot number is #9005860. The expiration date on the bottle is listed as EXP: 1282020.

Brand
Nexagen
Product
ACID RAIN ASS KICKING FAT DESTROYER APOCALYPSE LABZ; 45 CAPSULES; 1 DIETARY SUPPLEMENT; UPC 6 11138 28792 0
Category
Food

Based on the official FDA remedy

What to do — step by step

Stop consuming the product
Do not take any more capsules from the recalled bottles due to the inaccurate ingredient declaration.
Check your lot number
Confirm you have the specific affected item by verifying Lot #9005860 and UPC 6 11138 28792 0.
Contact the manufacturer
Reach out to Nexagen, LLC for further instructions on disposal or refunds since no specific remedy is currently listed in the record.

Where it went and when

Where it was distributed

Distributed in 6 states.

FDA distribution: “Product was distributed to the following states: AL, FL, GA, NM, TN & TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Florida, Georgia, New Mexico, Tennessee, Texas.

Recall timeline

FDA published this recall 2 months after the firm started it.

May 28, 2019Firm started the recall
Jul 24, 2019FDA classified it Class II
Jul 31, 2019Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/17416-nexagen-recalls-acid-rain-dietary-supplement-due-to-labeling-errors">Nexagen Recalls Acid Rain Dietary Supplement Due to Labeling Errors (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #F-1942-2019 (May 28, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1942-2019 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.