GE Pharma Recalls Creafuse Fruit Punch for DMAA Content
GE Pharma LLC is recalling Creafuse Fruit Punch, 600 Grams, because the product contains 1,3 dimethylamylamine (DMAA).
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classified this recall as Class II, which corresponds to a 'Severe' severity score under the rubric.
Plain-English summary
GE Pharma LLC is recalling 480 units of Creafuse Fruit Punch, 600 Grams, with code 4570. The recall was initiated because the product contains 1,3 dimethylamylamine (DMAA).
The affected product was distributed nationwide and worldwide. The agency has classified this recall as Class II.
Consumers who have this product should stop using it and follow the instructions provided by the recalling firm.
The recalled product
- Product
- Creafuse Fruit Punch, 600 Grams
- Manufacturer
- GE PHARMA LLC -
- Category
- Food — Supplements
- Hazard
- Affected units
- 480
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 4570
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by GE PHARMA LLC - under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · GE PHARMA LLC -
See all →- SevereGE Pharma Recalls Creafuse Grape Due to DMAA Contamination
FDA (Food) · 2013-11-13
Same hazard · unapproved ingredient
See all →- Severe
- HighAlpha Test supplement capsules recalled for unapproved cathine ingredient
FDA (Food) · 2025-02-05
- HighTruvy Boost Dietary Supplement Kit Recalled for Unapproved Ingredients
FDA (Food) · 2023-05-31
- ModerateDietary supplement Tight! Xtreme Reloaded recalled for unapproved ingredient
FDA (Food) · 2021-06-30
- SevereFDA Recalls PremierZen Black 5000 for Unapproved Tadalafil
FDA (Drugs) · 2021-05-26
Similar recalls
- SevereNaturecom Recalls DMAA Powder Due to Potential Presence of 1,3-Dimethylamylamine
FDA (Food) · 2016-12-28
- HighProSupps Recalls Dr. Jekyll Fruit Punch for Unapproved Ingredient Picamilon
FDA (Food) · 2017-10-11
- SevereBeta Labs Recalls Phentylene Dietary Supplement Containing DMAA
FDA (Food) · 2014-09-03
- SevereBeta Labs Recalls PHEnFX Dietary Supplement Containing Unapproved DMAA
FDA (Food) · 2014-09-03
- ModerateProSupps Recalls Dr. Jekyll 30 Fruit Punch for Mislabeling
FDA (Food) · 2017-07-05
- SevereMira Health Recalls Bolt Fat Incenerator Capsules Due to DMAA
FDA (Food) · 2014-02-19