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FDA recall record

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

Recall F-0766-2017Class IITerminatedNovember 8, 2016

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of July 29, 2017. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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

Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • 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

Code information listed by FDA

1607016, EXP 07/2018

Distribution and firm information

Recalling firm listed by FDA: Chaos and Pain

Firm location listed by FDA: Birmingham, AL, United States

Distribution reported by FDA: Nationwide, China, Germany, Norway, UK, Canada, Ireland, Italy, Australia, New Zealand, Hong Kong, Croatia

Product quantity listed by FDA: 277 units

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.