“Nutralliance MCT Powder 50% Recall: Undeclared Milk Allergen Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13465-nutralliance-mct-powder-50-recall-undeclared-milk-allergen-risk. Based on FDA recall #F-0613-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0613-2022%22&limit=1).
The FDA announced on Dec. 23, 2021, that Nutralliance Inc. is recalling Medium Chain Triglyceride (MCT) Powder 50% from Coconut due to undeclared milk allergens. The agency stated the recall addresses a Class I hazard.
How to tell if you have it
Brand: Nutralliance
Product: Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim
Packaging: 20 kilogram brown bags with plastic inner lining
Lot Numbers: MCT50190001 through MCT50190026
Distribution: CA, NV, NJ, NY, FL
The hazard
The product contains undeclared milk allergens. The FDA classified the recall as Class I, indicating a high risk of adverse health consequences.
Context
GovInfoNow's records show Nutralliance Inc has one other recall on record since April 30, 2021, involving MCT Powder 50% and milk allergen risks. Other recent recalls of similar products include Imu-Tek Immuno-5 Colostrum Powder (Nov. 25, 2025), Marquez Brothers Horchata Powder (April 7, 2026), and Wawa Fruit Punch Pint (April 2, 2026).
How to tell if you have this one
Check for 20kg brown bags labeled 'Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim'. Look for lot numbers starting with MCT50190001 to MCT50190026.
Brand
Nutralliance
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for lot numbers starting with MCT50190001 to MCT50190026 on the packaging.
Where it went and when
Where it was distributed
Distributed in 5 states.
Listed by the agency
Not listed
FDA distribution: “CA, NV, NJ, NY, FL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Nevada, New Jersey, New York.
Recall timeline
FDA terminated this recall 11 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-0613-2022 (December 23, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0613-2022 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.