Black Bean Bonanza Tamales with Black Beans and Jack Cheese Ingredients: Organic Corn Flour Masa, Black Beans, Jack Che
Summary
The FDA issued a Class II for Black Bean Bonanza Tamales with Black Beans and Jack Cheese Ingredients: Organi by Prima Vera Nueva, Inc.. Reason: Potential contamination with biological hazards (Listeria monocytogenes)..
Details
Source
Food Recall
External ID
H-0431-2026
Action Date
2026-02-04
Status
Terminated
Category
food
Product Description
Black Bean Bonanza Tamales with Black Beans and Jack Cheese Ingredients: Organic Corn Flour Masa, Black Beans, Jack Cheese (Pasteurized Milk, Cheese Cultures, Salt, Enzymes), Salsa (Tomatoes, Onions, Chiles, Garlic & Cilantro), Butter, Non-GMO Corn, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and Monocalcium Phosphate). Microwave: In husk approx. 90 seconds per tamale. Steam: In husk approx. 15 minutes. Primavera 17070 Sonoma Hwy. Sonoma, CA 95476 (707) 939-9350 Perishable Keep Refrigerated Net Wt. 24oz. UPC: 748732000218
Lot/Code Info: UPC: 748732000218
Quantity Affected: 26,457 packages (4 tamales/package)
Reason for Recall
Potential contamination with biological hazards (Listeria monocytogenes).
Distribution
U.S. Distribution: CA, NV
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-12
Company
Sonoma, 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 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Prima Vera Nueva, Inc. has 10 FDA actions in our database, including 10 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 (Prima Vera Nueva, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Prima Vera Nueva, Inc. have FDA actions?
Prima Vera Nueva, Inc. has 10 FDA actions in our database, including 10 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0431-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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