PlainRecalls
CriticalClass ITerminated

FDA Food recall · Reported December 9, 2015

DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, UPC 606851551205

The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection.

Recall #
F-0332-2016
Affected scope
3554 bottles
Initiated
August 28, 2015
Compiled from official public sources by the editorial team.
Verify with FDA Food →
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Vrvk Nutraceuticals, LLC recalled DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles… - a critical-severity action.

DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles… was recalled by Vrvk Nutraceuticals, LLC in December 9, 2015. Reason: The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection.. Check the official notice for the remedy. Verify recall #F-0332-2016 with the FDA Food before acting.

The recall

Vrvk Nutraceuticals, LLC issued this critical-severity FDA Food recall-The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection..

Critical
severity level
Class I
classification
December 9, 2015
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0332-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-0332-2016) was formally reported on December 9, 2015, with the manufacturer initiating the action on August 28, 2015. It is classified under Critical severity (Class I), with a current status of Terminated. Vrvk Nutraceuticals, LLC is listed as the recalling firm, operating out of Orlando, FL. Federal records list the affected scope as 3554 bottles.

The documented reason for this recall is: The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection. Distribution data in the federal record shows the product reached: Nationwide and Puerto Rico. 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, 6 from FDA Food - 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.

Dietary Supplements recalls over time

Where this recall sits in its category - 2,002 dietary supplements recalls on record

-1000100200300400 20072010201320162019202220252026 9
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Critical

Affected scope

3554 bottles

Related Recalls

6

6 from same agency

Product description

DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, UPC 606851551205

Reason for recall

The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number F-0332-2016
Date reported December 9, 2015
Date initiated August 28, 2015
Recalling firm Vrvk Nutraceuticals, LLC
Firm location Orlando, FL
Affected scope 3554 bottles
Distribution Nationwide and Puerto Rico

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.

  • Check the recall number (F-0332-2016) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next

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.

Frequently Asked Questions

What product was recalled?
DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, UPC 606851551205. Recalled by Vrvk Nutraceuticals, LLC. Units affected: 3554 bottles.
Why was this product recalled?
The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection.
Which agency issued this recall?
This recall was issued by the FDA Food on December 9, 2015. Severity: Critical. Recall number: F-0332-2016.
Where was the recalled product distributed?
Distribution: Nationwide and Puerto Rico.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-0332-2016) 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.

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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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 December 9, 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.