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FDA Food Verify with FDA Food → Moderate Class II Terminated

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

Reported: June 3, 2015 Initiated: April 9, 2015 #F-2323-2015 18,000 - 19,000 units units

Uber Vita LLC issued this FDA Food recall on June 3, 2015. Classified as Moderate severity (Class II). Approximately 18,000 - 19,000 units units are affected. The recall was issued because: It has come to the attention of Ubervita LLC that a packaging error has occurred with a product exclusively made for Wa…. This recall notice is sourced from official FDA Food enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

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 indicate 18,000 - 19,000 units units are affected, placing this recall in the million-unit bracket that typically triggers nationwide consumer alerts and retailer sweeps.

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.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 11 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

18,000 - 19,000 units

Related Recalls

6

0 from same agency

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

Reason for Recall

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

Details

Recalling Firm
Uber Vita LLC
Units Affected
18,000 - 19,000 units
Distribution
Nationwide to Wal-Mart only
Location
Manson, WA

Recall Profile

Structured summary of the FDA Food recall record
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
Units affected 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.

Scale of Impact

18,000 - 19,000 units units affected — million-unit bracket.

Regional (<10K units)
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units) ✓ This recall

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

Frequently Asked Questions

What product 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. Recalled by Uber Vita LLC. Units affected: 18,000 - 19,000 units.
Why was this product 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
Which agency issued this recall?
This recall was issued by the FDA Food on June 3, 2015. Severity: Moderate. Recall number: F-2323-2015.
Where was the recalled product distributed?
Distribution: Nationwide to Wal-Mart only.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-2323-2015) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).