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RECALLING FIRM / COMPANY

Chaos and Pain Recalls

Are there any recent recalls involving Chaos and Pain?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

3 FDA product recordsLatest initiation: Nov 8, 2016

Same product name.
Different batch.
Check the label.

All recall records involving Chaos and Pain

Initiated in 2016. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

3 recall recordsPage 1 of 1
Class II
FDA status: Terminated

CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT,…

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

Labeling / mislabelingView details →
Class II
FDA status: Terminated

CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY…

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…

Labeling / mislabelingView details →
Class II
FDA status: Terminated

CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT.…

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…

Labeling / mislabelingView details →

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Same product name. Different batch. Details matter.

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