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Class IITerminated in FDA datasetRecall initiated Apr 9, 2015

UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY SUPPLEMENT. The product…

Recalling firm: Uber Vita LLC

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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 4, 2016.

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Compare the exact product and package details with the label you have.

ProductUBERVITA 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
UPC700115352772

FDA code information

Lot 20050 Expiration date 2-28-2018

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Full FDA record and distribution details

Original 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

Extracted codes and context

TypeCode / valueContext
UPC700115352772box with gold and chrome foil. Bottle inside is black and red in color. UPC 7 00115 35277 2
expiration2-28-2018Lot 20050 Expiration date 2-28-2018

Original FDA recall reason

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

Recall details

Recall number
F-2323-2015
Event ID
70978
FDA status
Terminated
Initiated
Apr 9, 2015
Reported
Jun 3, 2015
Classified
May 27, 2015
Terminated
Apr 4, 2016
Quantity
18,000 - 19,000 units
Location
Manson, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide to Wal-Mart only

FDA source record · F-2323-2015

Data updated September 16, 2026. View official FDA data ↗

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