Arepas de Chocolo, Abuelas Food Company, Delicias de la Abuela's, Net Weight: 22.5oz. (638g), 5 units per package, Vacuu
Summary
The FDA issued a Class II for Arepas de Chocolo, Abuelas Food Company, Delicias de la Abuela's, Net Weight: 22 by DELICIAS DE LA ABUELA INC. Reason: Undeclared allergen: Soy lecithin, less than 2%.
Details
Source
Food Recall
External ID
F-0708-2025
Action Date
2025-04-23
Status
Terminated
Category
food
Product Description
Arepas de Chocolo, Abuelas Food Company, Delicias de la Abuela's, Net Weight: 22.5oz. (638g), 5 units per package, Vacuum seal packages and twist tie bags, KEEP REFRIGERATED. UPC 850283002037
Lot/Code Info: UPC 850283002037
Quantity Affected: Total of 1504 units- Retail: 604 units and Food Service/ Restaurants: 900
Reason for Recall
Undeclared allergen: Soy lecithin, less than 2%
Distribution
Florida
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-18
Company
Riviera Beach, FL
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 25 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (DELICIAS DE LA ABUELA INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DELICIAS DE LA ABUELA INC have FDA actions?
This is the only FDA action we have on record for DELICIAS DE LA ABUELA INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0708-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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