MIGHTYLICIOUS Vegan Oatmeal Coconut Cookies Gluten-Free, Dairy-Free, Allergen Friendly, Egg-Free, Non-GMO, Kosher, Pre
Summary
The FDA issued a Class I for MIGHTYLICIOUS Vegan Oatmeal Coconut Cookies Gluten-Free, Dairy-Free, Allergen by Mightylicious Inc.. Reason: Undeclared Milk.
Details
Source
Food Recall
External ID
H-0066-2025
Action Date
2025-07-02
Status
Terminated
Category
food
Product Description
MIGHTYLICIOUS Vegan Oatmeal Coconut Cookies Gluten-Free, Dairy-Free, Allergen Friendly, Egg-Free, Non-GMO, Kosher, Preservative-Free Snack Option for a Guilt-Free Treat - 6.5 Oz, Stand-up pouch, 6 bags per case . UPC: -0085000955838
Lot/Code Info: BBD: 9/19/25 Lot Code: 2353
Quantity Affected: 330 cases
Reason for Recall
Undeclared Milk
Distribution
The recalled product was distributed to the following states: RI, IL, NY
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-10
Company
Wood-Ridge, NJ
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 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Mightylicious Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mightylicious Inc. have FDA actions?
This is the only FDA action we have on record for Mightylicious Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0066-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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