Nutralliance Inc Recall: Ingredient tested positive for milk allergen.

🇺🇸 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-0794-2021

Event ID

87846

Status

Terminated

Classification

Class I

Company

Nutralliance Inc

Product description

Medium Chain Triglyceride (MCT) Powder 70% 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

350 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: MCT70190027; MCT70190028; MCT70190029; MCT70190038; MCT70190039; MCT70190040; MCT70190041; MCT70190042

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.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

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?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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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