Chaos and Pain Recall: Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance. - F-0766-2017

🇺🇸 United States

1. November 8, 2016 - Recall initiated
2. December 28, 2016 - Reported by source
3. July 29, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0766-2017

Event ID

75907

Status

Terminated

Classification

Class II

Company

Chaos and Pain

Product description

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

Quantity

277 units

Reason

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

Recall initiation date

November 8, 2016

Report date

December 28, 2016

Classification date

Not published in this source record

Termination date

July 29, 2017

Distribution pattern

Nationwide, China, Germany, Norway, UK, Canada, Ireland, Italy, Australia, New Zealand, Hong Kong, Croatia

UPC, lot, and code information

UPC 1056331460; 1607016, EXP 07/2018

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Chaos and Pain

Other recalls from Chaos and Pain

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of July 29, 2017.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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