76%

Fewer recalls than
Supplements & Specialty peers

Chaos and Pain — FDA Recall History & Enforcement Records

Established Player · Supplements & Specialty

Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.

As of July 16, 2026, Chaos and Pain has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 8 Nov 2016. Chaos and Pain is categorized under Supplements & Specialty based on their predominant recall history.

3
Total FDA recalls
9.9
Years in FDA database
0.3
Recalls per year
3,537 days(9.7 yrs)
Since last recall
0.0%
Class I (life-threatening)
0.3 recalls/yr vs Supplements & Specialty avg 2.3/yrWell Below Average

Recall activity over time for Chaos and Pain

How serious are Chaos and Pain recalls?

FDA recall classifications by severity

Class I (Life-threatening)
0.0% (0 recalls)
Class II (Moderate risk)
100.0% (3 recalls)
Class III (Minor violation)
0.0% (0 recalls)

Full FDA recall history for Chaos and Pain

All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first

Date Product Reason Class & Status
8 Nov 2016Official FDA Notice CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT, NE Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance. Class IITerminated
10 Aug 2016Official FDA Notice CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 1 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 labe Class IITerminated
10 Aug 2016Official FDA Notice CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY SUPPLEMENTS, 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 labe Class IITerminated

Where have Chaos and Pain recalls occurred?

States affected across all recorded FDA enforcement actions

Nationwide

Where does this recall data come from?

Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.

Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.

To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.

© 2026 FoodRecallFinder.com | Turnkey Trading Unlimited LLC. All rights reserved. FDA recall data sourced from openFDA.gov.

How we calculate these metrics →