La Michoacana Coconut Con Crema Single Serve Paleta 3.75oz UPC: 7-67778-00001-3
Summary
The FDA issued a Class II for La Michoacana Coconut Con Crema Single Serve Paleta 3.75oz UPC: 7-67778-00001-3 by Tropicale Foods, LLC. Reason: Product label includes the ingredient CREAM but does not include Milk as the source..
Details
Source
Food Recall
External ID
H-0458-2025
Action Date
2025-08-20
Status
Ongoing
Category
food
Product Description
La Michoacana Coconut Con Crema Single Serve Paleta 3.75oz UPC: 7-67778-00001-3
Lot/Code Info: Best By Date: 10/3/2026 - 5/3/2027
Quantity Affected: 74,654 units
Reason for Recall
Product label includes the ingredient CREAM but does not include Milk as the source.
Distribution
Nationwide distribution
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-25
Company
Ontario, CA
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 113 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tropicale Foods, LLC has 14 FDA actions in our database, including 14 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 (Tropicale Foods, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tropicale Foods, LLC have FDA actions?
Tropicale Foods, LLC has 14 FDA actions in our database, including 14 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0458-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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