Severity
Moderate
FDA Food recall · Reported June 3, 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 less than 30 units of it…
Uber Vita LLC recalled UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY SUPPLEMENT. The p… - a moderate-severity action.
UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY SUPPLEMENT. The p… was recalled by Uber Vita LLC in June 3, 2015. Reason: It has come to the attention of Ubervita LLC that a packaging error has occurred with a product exclusively m…. Check the official notice for the remedy. Verify recall #F-2323-2015 with the FDA Food before acting.
The recall
Uber Vita LLC issued this moderate-severity FDA Food recall-It has come to the attention of Ubervita LLC that a packaging error has occurred with a product exclusively m….
Sourced from official FDA Food enforcement records. Verify recall #F-2323-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-2323-2015) was formally reported on June 3, 2015, with the manufacturer initiating the action on April 9, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Uber Vita LLC is listed as the recalling firm, operating out of Manson, WA. Federal records list the affected scope as 18,000 - 19,000 units.
The documented reason for this recall is: 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 vi… Distribution data in the federal record shows the product reached: Nationwide to Wal-Mart only. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
18,000 - 19,000 units
Related Recalls
6
0 from same agency
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
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
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2323-2015 |
| Date reported | June 3, 2015 |
| Date initiated | April 9, 2015 |
| Recalling firm | Uber Vita LLC |
| Firm location | Manson, WA |
| Affected scope | 18,000 - 19,000 units |
| Distribution | Nationwide to Wal-Mart only |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported June 3, 2015. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.