Class IITerminatedVoluntary: Firm initiated

DELICIAS DE LA ABUELA INC: food recall F-0708-2025

DELICIAS DE LA ABUELA INC of Riviera Beach, FL recalled Arepas de Chocolo, Abuelas Food Company, Delicias de la Abuela's, Net Weight: 22.5oz. (638g), 5 units per package,… Reason: Undeclared allergen: Soy lecithin, less than 2%. The FDA listed it as Class II in its Enforcement Report dated Apr 23, 2025; distribution: Florida.

Record status as published: Terminated (terminated Aug 6, 2025). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
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
Product quantity
Total of 1504 units- Retail: 604 units and Food Service/ Restaurants: 900
Reason for recall
Undeclared allergen: Soy lecithin, less than 2%
Codes, lots and dates on the package
UPC 850283002037
Distribution pattern
Florida
Recalling firm
DELICIAS DE LA ABUELA INC, Riviera Beach, FL
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmMar 18, 2025
Classified by the FDAApr 14, 2025
Published in the Enforcement ReportApr 23, 2025
TerminatedAug 6, 2025

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0708-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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