Nutralliance Inc Recall: Ingredient tested positive for milk allergen. - F-0793-2021

🇺🇸 United States

1. April 30, 2021 - Recall initiated
2. July 28, 2021 - Reported by source
3. February 28, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0793-2021

Event ID

87846

Status

Terminated

Classification

Class I

Company

Nutralliance Inc

Product description

Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim packaged in 20 kilogram brown bags with plastic inner lining for bulk sale to supplement manufacturers. Exclusively Distributed by Nutralliance / Manufactured by Bio-gen Extracts Pvt. Ltd. Store tightly sealed container at room temperature away from moisture and direct sunlight.

Quantity

794 bags

Reason

Ingredient tested positive for milk allergen.

Recall initiation date

April 30, 2021

Report date

July 28, 2021

Classification date

Not published in this source record

Termination date

February 28, 2023

Distribution pattern

Nationwide. Canada.

UPC, lot, and code information

Lot Numbers: MCT50200001; MCT50200002; MCT50200003; MCT50200004; MCT50200005; MCT50200006; MCT50200007; MCT50200008; MCT50200009; MCT50200010; MCT50200011; MCT50200012; MCT50200013; MCT50200014; MCT50200015; MCT50200030

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 87846 with 1 other product entry in Public Health Trace.

Responsible company: Nutralliance Inc

Other recalls from Nutralliance Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of February 28, 2023.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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