Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 9, 2015 (12 years ago)

Ubervita Lose Weight Fast W700 Thermogenic Hyper-Metabolizer Dietary Supplement recall

Recalled by Uber Vita LLC · Manson, WA, United States

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

Why it was recalled

It has come to the attention of Ubervita LLC that a packaging error has occurred with a product exclusively made for Walmart Stores. This issue applies to less than 30 units of its W700 Lose Weight product. While the vitamin bottles are labeled accurately, less than 30-bottles of UBERTEST TESTOSTERONE EXTREME BOOST FOR MEN were placed into W700 Lose Weight boxes. The outer box is labeled as the W7

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY SUPPLEMENT. The product has an outer box which contains a labeled bottle. This is a bright red box with gold and chrome foil. Bottle inside is black and red in color. UPC 7 00115 35277 2

Quantity: 18,000 - 19,000 units

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.

Lot 20050 Expiration date 2-28-2018

Where it was sold

Nationwide.

FDA's distribution note: Nationwide to Wal-Mart only

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
Uber Vita LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 9, 2015
In FDA report of
Jun 3, 2015
Terminated
Apr 4, 2016
FDA recall number
F-2323-2015 · event 70978
Official record
FDA enforcement report search

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