CANNIBAL FEROX AMPED — Class II food recall F-0766-2017
Terminated recall by Chaos and Pain, reported 2016-12-28, distributed nationwide. Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a
| Recall number | F-0766-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Chaos and Pain, Birmingham, AL, United States |
| Recall initiated | 2016-11-08 |
| Classified | 2016-12-21 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2017-07-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CN, DE, GB, HK, HR, IE, IT, NO, NZ |
| Quantity | 277 units |
| Reason classes | undeclared allergen, labeling |
| Expiration dates | 2018-07 |
Product
CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT, NET. WT. 9.9 OZ (280g), Chaos and Pain, UPC 1056331460
Reason for recall
Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0766-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.