Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
Dr. Venessa's Formulas Ultimate Antioxidant Tablets Dietary Supplement recall
Recalled by VRVK Nutraceuticals, LLC · Orlando, FL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The dietary supplement contains undeclared milk and crustacean shellfish based on FDA's inspection.
Undeclared allergens: Milk Shellfish
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, UPC 606851551205
Quantity: 3554 bottles
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot Number 132415 (expiration date 05/16) and Lot Number 141381 (expiration date 06/17)
Where it was sold
Nationwide.
Puerto Rico
FDA's distribution note: Nationwide and Puerto Rico
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, shellfish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- VRVK Nutraceuticals, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 28, 2015
- In FDA report of
- Dec 9, 2015
- Terminated
- Jun 13, 2018
- FDA recall number
- F-0332-2016 · event 72074
- Official record
- FDA enforcement report search
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