Lower riskFood recall · FDA · Published December 3, 2021
BUBS Naturals Fountain of Youth Formula Recall: Undeclared Milk in Supplement
BUBS Naturals recalls fountain of youth formula due to undeclared milk in MCT oil powder. Consumers should check lot numbers and contact the company for details.
“BUBS Naturals Fountain of Youth Formula Recall: Undeclared Milk in Supplement.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13689-bubs-naturals-fountain-of-youth-formula-recall-undeclared-milk-in. Based on FDA recall #F-0354-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0354-2022%22&limit=1).
The FDA announced on Dec. 3, 2021, that Slayer Forever, LLC dba BUBS Naturals voluntarily recalled its Fountain of Youth Formula supplements due to undeclared milk allergens. The recall affects 12,774 units distributed nationwide.
How to tell if you have it
Brand: BUBS Naturals
Product: Fountain of Youth Formula; Collagen Protein; Support for Hair, Skin & Nails; Biotin, Antioxidant, Vitamin C; Maqui Berry Net Wt. 10.16 oz. (288 g)
Lot # 04230401, Exp. 05/28/2022
Lot # 15908501. Exp. 07/13/2023
The hazard
The supplement contains undeclared milk from the MCT oil powder ingredient, posing a risk to individuals with milk allergies.
Context
GovInfoNow's records show Slayer Forever, LLC dba BUBS Naturals has one other recall on record since May 7, 2021, involving undeclared milk allergens in MCT Oil Powder. Other recent recalls of similar products include Imu-Tek Immuno-5 Colostrum Powder Recall (Nov. 25, 2025), Nuts.com Espresso Malted Milk Balls Recall (March 10, 2026), and Loard's Peppermint Ice Cream Recall (April 15, 2026).
How to tell if you have this one
Check the product label for lot numbers 04230401 (expiring May 28, 2022) or 15908501 (expiring July 13, 2023). The product is sold in 10.16 oz. (288 g) containers.
Brand
BUBS Naturals
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for lot numbers 04230401 (expiring May 28, 2022) or 15908501 (expiring July 13, 2023) on the container.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0354-2022 (December 3, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0354-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.