CLASS II Food recall · Reported 13 Nov 2013 · FDA Enforcement Report

Creafuse Grape recalled by Ge Pharma Llc -

Ge Pharma Llc - is recalling Creafuse Grape, distributed nationwide in the US. The recall was initiated on 1 Sep 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes4568
Quantity recalled480 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0116-2014
FDA event ID
66236
Recalling firm
Ge Pharma Llc -, North Haven, CT
Classification
Class II
Status
Terminated
Recall initiated
1 Sep 2013
FDA classified
5 Nov 2013
Reported
13 Nov 2013
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Product category
Grapes

Timeline

1 Sep 2013Recall initiated by company
5 Nov 2013Classified by FDA+65 days
13 Nov 2013Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains 1,3 dimethylamylamine (DMAA)

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

Creafuse Grape, 600 Grams

Where it was distributed

Nationwide and Worldwide

Nationwide

Questions about this recall

Is Creafuse Grape recalled?

Yes. Ge Pharma Llc - recalled Creafuse Grape on 1 Sep 2013. The recall is Class II and its status is Terminated. Recall number F-0116-2014.

Why was it recalled?

Product contains 1,3 dimethylamylamine (DMAA)

Which lots are affected?

4568

Where was it sold?

Nationwide and Worldwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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