Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 2, 2013 (14 years ago)

Growth Factor Complex 200 GFC 200 recall

Recalled by EonNutra, LLC · Colorado Springs, CO, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Eon Nutra, LLC is recalling certain SOTO Supplements GFC 200 because the liquid dietary supplement products may be contaminated with various types of bacteria.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Growth Factor Complex 200 GFC 200, Dietary Supplement 2 Fl Oz, Manufactured for: Soto Supplements P.O. Box 75774 Colorado Springs, CO 80237, Instructions: Place drops under your tongue for 2 min then swallow. Do not eat or drink for 15 min. Only approved for distribution from Authorized Distributors/Retailers, pharmaceutical laboratories and governmental research facilities.

Quantity: 199 x 2 oz bottles

Food: Dietary supplements

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.

SRK91512; SRK92112; SRK92512; SRK102312; SRK11412; SRK111912.

Where it was sold

Nationwide.

Arkansas California Colorado Florida Georgia Michigan Missouri North Carolina North Dakota Nebraska New Jersey South Carolina Tennessee Texas Utah Wisconsin

FDA's distribution note: Nationwide, AR, CA, CO, FL, GA, IO, MI, MO, NC, ND, NE, NJ, SC, TN, TX, UT, WI

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
EonNutra, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 2, 2013
In FDA report of
Feb 6, 2013
Terminated
Feb 12, 2013
FDA recall number
F-0937-2013 · event 64011
Official record
FDA enforcement report search

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