RecallHawk
Class II Recall

Simply Goodfats Creamy MCT Vanilla MCT Oil Powder 10.5 OZ packaged White HDPE Plastic. UPC Code: 857826008648 Expira

Naomi Whittel Brands, LLC

Summary

The FDA issued a Class II for Simply Goodfats Creamy MCT Vanilla MCT Oil Powder 10.5 OZ packaged White HDPE P by Naomi Whittel Brands, LLC. Reason: Undeclared milk allergen.

Details

Source

Food Recall

External ID

F-0800-2022

Action Date

2022-02-16

Status

Terminated

Category

food

Product Description

Simply Goodfats Creamy MCT Vanilla MCT Oil Powder 10.5 OZ packaged White HDPE Plastic. UPC Code: 857826008648 Expiration dates: 8/31/2021 8/31/2022 2/28/2022

Lot/Code Info: Lots 907044, 908021, and 002051

Quantity Affected: 1,647 units

Reason for Recall

Undeclared milk allergen

Distribution

Distributed to online customers in the US.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-01-26

Company

Naomi Whittel Brands, LLC

Tysons Corner, VA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 115 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Naomi Whittel Brands, LLC has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Naomi Whittel Brands, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Naomi Whittel Brands, LLC have FDA actions?

Naomi Whittel Brands, LLC 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-0800-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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