Chaos and Pain Dietary Supplements Recall: Unapproved Ingredients in Energy Products
Chaos and Pain recalls several energy supplements due to unlisted ingredients violating EU dietary supplement regulations. Products contain 750mg Agmatine and 50mg 1,3-Dimethylbutylamine per serving, which are not permitted in EU supplements.
Lower-risk recall
The products are being recalled because they contain 750 mg of Agmatine and 50 mg 1,3 Dimethylbutylamine per serving which is not declared on the label. 1,3 Dimethylbutylamine is not permitted for use in dietary supplements in the EU.
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What happened, in plain English
Chaos and Pain is recalling several energy supplements because they contain unlisted ingredients that are not allowed in EU dietary supplements. This could pose a risk if the products are used as intended. Read more at govinfonow.com/recall/23476-chaos-and-pain-dietary-supplements-recall-unapproved-ingredients-in-energy.
Source Summary by GovInfoNow · govinfonow.com/recall/23476-chaos-and-pain-dietary-supplements-recall-unapproved-ingredients-in-energy · Updated October 9, 2026 · FDA enforcement record: FDA #F-0082-2017
Cite this page
“Chaos and Pain Dietary Supplements Recall: Unapproved Ingredients in Energy Products.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23476-chaos-and-pain-dietary-supplements-recall-unapproved-ingredients-in-energy. Based on FDA recall #F-0082-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0082-2017%22&limit=1).
Why it’s dangerous
The products contain 750mg of Agmatine and 50mg of 1,3-Dimethylbutylamine per serving, which are not permitted in EU dietary supplements. These ingredients were not declared on the product labels, potentially violating EU regulations.
Who’s affected
Owners of the recalled energy supplements are likely to be consumers who purchased these products from retailers. People using these supplements for fitness purposes may be at higher risk due to the unapproved ingredients.
How to tell if you have this one
Check for the product names: CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, or Chaos and Pain. The products were sold in 10.5 oz (300g) containers with UPC 610563314669 and lot number 1607018, expiring July 2018.
- Brand
Chaos and Pain- Product
CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
UK
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0081-2017 | CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314652; Lot 1607017 EXP 07/18 | 1000 units |
| F-0082-2017 | CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314669; Lot 1607018 EXP 07/18 | N/A |
What to do — step by step
Check Product Details
Verify if your product matches the described names and UPC 610563314669 with lot number 1607018.
How this recall unfolded
Recall timeline
FDA terminated this recall 5 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-0082-2017 (August 10, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0082-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.