The Recall Desk
SevereFDA (Food)·F-0116-2014·Announced 2013-11-13

GE Pharma Recalls Creafuse Grape Due to DMAA Contamination

GE Pharma LLC is recalling 480 units of Creafuse Grape, 600 Grams, because the product contains 1,3 dimethylamylamine (DMAA).

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class II, which corresponds to a Severe severity score under the rubric.

Plain-English summary

GE Pharma LLC is recalling 480 units of Creafuse Grape, 600 Grams. The recall was initiated because the product contains 1,3 dimethylamylamine (DMAA).

The affected product is identified by code 4568. The recall covers distribution nationwide and worldwide.

Consumers should stop using the product and contact the recalling firm for further instructions.

The recalled product

Product
Creafuse Grape, 600 Grams
Manufacturer
GE PHARMA LLC -
Category
Food — Supplement
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)

  • 4568

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 -

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Same hazard · dmaa contamination

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