Data / Product recalls / Chaos and Pain
Chaos and Pain: 2 recalls in 2016 (FDA)
Chaos and Pain, Birmingham, AL, is named in 2 recalls in 2016: all from the FDA. The latest, on December 28, 2016, covers CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT.... Hazard: Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance. Source: FDA F-0766-2017.
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- Country
- United States
- Location
- Birmingham, AL
- Agencies
- U.S. Food and Drug Administration
- First recall
- October 19, 2016
- Latest recall
- December 28, 2016
Recalls
Each recall is listed once, with the role this firm has in it. Roles: recalling firm (2).
| Date | Agency | Product | Hazard | Units | Remedy | Sold at | Role | Source |
|---|---|---|---|---|---|---|---|---|
| December 28, 2016 | FDA | CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT, NET. WT. 9.9 OZ (280g), Chaos... | Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance. | 277 units | Voluntary recall, Class II, terminated | Recalling firm | accessdata.fda.gov | |
| October 19, 2016 | FDA | CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC... and 1 more product | 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 label. 1,3 Dimethylbutylamine is not permitted for use in dietary supplements in the EU. | 1000 units (first of 2 products) | Voluntary recall, Class II, terminated | Recalling firm | accessdata.fda.gov |
By agency
| Agency | Recalls | Latest |
|---|---|---|
| U.S. Food and Drug Administration | 2 | December 28, 2016 |
Categories
| Category | Recalls |
|---|---|
| Dietary supplements | 2 |
Where each agency publishes its recalls
Updated December 28, 2016. Read from U.S. Food and Drug Administration recall data. CC0 1.0 (openFDA). Recalls are as the agencies published them: the CPSC, FDA (food enforcement reports) and NHTSA. A firm is one firm only when its exact name and country match; the CPSC and FDA print no firm ID. Stores are listed only when the agency's sold-at text names them, and an agency often adds that more stores sold the product. Categories are grouped by SpecStream from the words in the agency's title and product text. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.