Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim packaged in 20 kilogram brown bags with plastic inner
Summary
The FDA issued a Class I for Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim packaged in 2 by Nutralliance Inc. Reason: Undeclared allergen; milk..
Details
Source
Food Recall
External ID
F-0613-2022
Action Date
2022-02-02
Status
Terminated
Category
food
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. Distributed exclusively by Nutralliance.
Lot/Code Info: Lot Numbers: MCT50190001 MCT50190002 MCT50190003 MCT50190004 MCT50190005 MCT50190006 MCT50190007 MCT50190008 MCT50190009 MCT50190010 MCT50190011 MCT50190012 MCT50190013 MCT50190014 MCT50190015 MCT50190016 MCT50190017 MCT50190018 MCT50190019 MCT50190020 MCT50190021 MCT50190022 MCT50190023 MCT50190024 MCT50190025 MCT50190026
Quantity Affected: 727.5 bags @ 20kg
Reason for Recall
Undeclared allergen; milk.
Distribution
CA, NV, NJ, NY, FL
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-23
Company
Yorba Linda, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 117 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Nutralliance Inc has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Nutralliance Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Nutralliance Inc have FDA actions?
Nutralliance Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0613-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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