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GE PHARMA LLC -
FDA recall F-0116-2014 · Class II · reported 2013-11-13 · Terminated
- Product
- Creafuse Grape, 600 Grams
- Reason
- Product contains 1,3 dimethylamylamine (DMAA)
- Quantity
- 480 units
- Distribution
- Nationwide and Worldwide
- Firm location
- CT, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Recall started
- 2013-09-01
- Terminated
- 2015-11-18
- Code info
- 4568
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.