FDA recall record

Uber Vita UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER recall — FDA F-2323-2015

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…

Class IIclassification
F-2323-2015official record ID
Jun 3, 2015report date

Recall record at a glance

Official recordF-2323-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmUber Vita LLC
Report dateJun 3, 2015
Recall initiation dateApr 9, 2015
Quantity18,000 - 19,000 units
LocationManson, WA, United States

Official product description

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

Why the product 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

Distribution information

Nationwide to Wal-Mart only

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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