BUBS Naturals MCT OIL Powder
Reason Firm was notified by supplier of Medium Chain Triglycerides (MCT) that it contained undeclared milk allergens.
BUBS Naturals Fountain of Youth Formula recall
Recalled by Slayer Forever, LLC dba BUBS Naturals · Encinitas, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Supplement contains undeclared milk from MCT oil powder ingredient.
Undeclared allergen: Milk
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
BUBS Naturals Fountain of Youth Formula; Collagen Protein; Support for Hair, Skin & Nails; Biotin, Antioxidant, Vitamin C; Maqui Berry Net Wt. 10.16 oz. (288 g)
Quantity: 12,774 units
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 # 04230401, Exp. 05/28/2022; Lot # 15908501. Exp. 07/13/2023
Where it was sold
Nationwide.
FDA's distribution note: Nationwide.
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; 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
- Slayer Forever, LLC dba BUBS Naturals
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 3, 2021
- In FDA report of
- Jan 5, 2022
- Terminated
- May 5, 2022
- FDA recall number
- F-0354-2022 · event 89145
- Official record
- FDA enforcement report search