BUBS Naturals recalls MCT oil powder supplements containing undeclared milk allergens. Consumers should check product codes and contact the company for details.
“BUBS Naturals MCT Oil Powder Recall: Undeclared Milk Allergens.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14544-bubs-naturals-mct-oil-powder-recall-undeclared-milk-allergens. Based on FDA recall #F-0847-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0847-2021%22&limit=1).
The FDA announced on May 7, 2021, that Slayer Forever, LLC dba BUBS Naturals voluntarily recalled BUBS Naturals MCT OIL Powder due to undeclared milk allergens. The firm notified the agency that the dietary supplement contained milk from its supplier.
How to tell if you have it
BUBS Naturals
MCT OIL Powder, Medium Chain Triglycerides from 100% virgin Coconut Oil
Dietary Supplement 10.6 oz
Gusset Bags
Lot codes MCT50200004 through MCT50200013
Expiration dates 1/22 and 5/22
The hazard
The recall involves undeclared milk allergens in the Medium Chain Triglycerides (MCT) oil powder ingredient. The FDA classified this as a Class I recall, indicating a high risk of adverse health consequences.
Context
GovInfoNow's records show Slayer Forever, LLC dba BUBS Naturals has one other recall on record since 2021-12-03. On 2021-12-03, the brand recalled its Fountain of Youth Formula for containing undeclared milk from an MCT oil powder ingredient. Other recent recalls of similar products include Imu-Tek Immuno-5 Colostrum Powder (2025-11-25), Nuts.com Espresso Malted Milk Balls (2026-03-10), and Marquez Brothers Horchata Powder (2026-04-07).
How to tell if you have this one
Check for product codes MCT50200004 through MCT50200013, which expire between January 2022 and May 2022. The product is sold in 10.6 oz. powder form as a dietary supplement.
Brand
BUBS Naturals
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Codes
Look for product codes MCT50200004 to MCT50200013 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide distribution through 2 distributors, Amazon and firm's online store.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3FDA terminated the recall
4Published in FDA’s Enforcement Report
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-0847-2021 (May 7, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0847-2021 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.