Chaos and Pain Dietary Supplement Recall: Unlabeled Prohibited Substance
Chaos and Pain recalls several dietary supplements for containing an unlabeled prohibited substance that may pose health risks. Consumers should check product labels and contact the company for details.
Recall notice
Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance.
Contact the company
What happened, in plain English
Chaos and Pain is recalling multiple dietary supplements that contain 1,3-dimethylbutylamine, a substance not listed on labels and prohibited by regulations. This could pose health risks to consumers using these products. Read more at govinfonow.com/recall/22916-chaos-and-pain-dietary-supplement-recall-unlabeled-prohibited-substance.
Source Summary by GovInfoNow · govinfonow.com/recall/22916-chaos-and-pain-dietary-supplement-recall-unlabeled-prohibited-substance · Updated October 8, 2026 · FDA enforcement record: FDA #F-0766-2017
Cite this page
“Chaos and Pain Dietary Supplement Recall: Unlabeled Prohibited Substance.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22916-chaos-and-pain-dietary-supplement-recall-unlabeled-prohibited-substance. Based on FDA recall #F-0766-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0766-2017%22&limit=1).
Why it’s dangerous
The product contains 1,3-dimethylbutylamine, a prohibited substance not declared on the label. This chemical is not approved for use in dietary supplements and could cause health issues if consumed.
Who’s affected
Anyone who owns or uses the recalled dietary supplements. People most at risk are those who have consumed the product without knowing it contains an unlabeled prohibited substance.
How to tell if you have this one
Check for the product names: CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH. The supplements were sold with a net weight of 9.9 oz (280g) and have specific UPC codes.
- Brand
Chaos and Pain- Product
CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT- Category
Food
What to do — step by step
Check Product Labels
Look for the product names and net weight of 9.9 oz (280g) on the label.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Nationwide, China, Germany, Norway, UK, Canada, Ireland, Italy, Australia, New Zealand, Hong Kong, Croatia” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-0766-2017 (November 8, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0766-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.