Why it was recalled
Product contains 1,3 dimethylamylamine (DMAA)
Product description
Creafuse Grape, 600 Grams
Lot numbers, UPCs & expiration codes
4568
Where it was sold
Nationwide and Worldwide
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0116-2014
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Sep 1, 2013
- FDA report date
- Nov 13, 2013
- Quantity
- 480 units
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- GE PHARMA LLC -
Original FDA data
Every field from FDA enforcement report F-0116-2014, exactly as published.
Show all FDA fields
- City
- North Haven
- State
- CT
- Status
- Terminated
- Country
- United States
- Event ID
- 66236
- Address
- 55 Middletown Ave Ste 2
- Code information
- 4568
- Postal code
- 06473-3936
- Report date
- Nov 13, 2013
- Product type
- Food
- Recall number
- F-0116-2014
- Classification
- Class II
- Recalling firm
- GE PHARMA LLC -
- Product quantity
- 480 units
- Termination date
- Nov 18, 2015
- Reason for recall
- Product contains 1,3 dimethylamylamine (DMAA)
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Creafuse Grape, 600 Grams
- Distribution pattern
- Nationwide and Worldwide
- Recall initiation date
- Sep 1, 2013
- Initial firm notification
- Center classification date
- Nov 5, 2013