Creafuse Fruit Punch
Reason Product contains 1,3 dimethylamylamine (DMAA)
Creafuse Grape recall
Recalled by Ge Pharma LLC - · North Haven, CT, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains 1,3 dimethylamylamine (DMAA)
The label gives no warning, so buyers cannot know about dangerous interactions with medicines they already take. All hidden drug ingredients recalls.
What was recalled
Creafuse Grape, 600 Grams
Quantity: 480 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
4568
Where it was sold
Nationwide.
FDA's distribution note: Nationwide and Worldwide
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Ge Pharma LLC -
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 1, 2013
- In FDA report of
- Nov 13, 2013
- Terminated
- Nov 18, 2015
- FDA recall number
- F-0116-2014 · event 66236
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.