MODERATE RISK
Terminated
F-0116-2014
Creafuse Grape, 600 Grams
Recalled by GE PHARMA LLC -
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
Reason for Recall
Product contains 1,3 dimethylamylamine (DMAA)
Product Details
Product Quantity
480 units
Product Type
Food
Code Info
4568
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Nationwide and Worldwide
Company Location
North Haven, CT, 06473-3936
Timeline
Report Date
11/13/2013
Recall Initiated
09/01/2013
Classification Date
11/05/2013
Termination Date
11/18/2015
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 29, 2026
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