Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 30, 2014 (13 years ago)

Mega Slim Herbal Appetite Management recall

Recalled by YoungYou International Inc · Tarzana, CA, United States

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

Why it was recalled

YoungYou International is voluntarily recalling Mega Slim Herbal Appetite Management, 30 capsules, sold from September 15, 2013 through January 23, 2014, because it was found to contain 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

Mega Slim Herbal Appetite Management, 30 Capsules Bottle. Product labeling reads in part:"MEGASLIM Herbal Appetite Management***30 Capsules***YoungYou Weight Loss Center***MegaSim Propriety Blend 590 mg, Garcinia Cambogia Extract, Green Tea, Aloe Ferox, L-Carnitine, Caralluma fimbriata Extract***Distributed by YoungYou International Inc. Earth Creation, USA (877) 496-8649 www.youngyoucorp.com***".

Quantity: 27 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.

No Lot Codes. Product sold/distributed September 15, 2013 through January 23, 2014. UPC code 7 36211 61409. Expiration date June 2014.

Where it was sold

FDA's distribution note: US and Canada.

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
YoungYou International Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 30, 2014
In FDA report of
Feb 26, 2014
Terminated
Nov 13, 2014
FDA recall number
F-1541-2014 · event 67402
Official record
FDA enforcement report search

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