Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 oz (226.8 g) boxes, 6/8oz boxes per case. UPC 07298100
Summary
The FDA issued a Class II for Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 oz (226.8 g) b by Rovira Biscuit Corporation. Reason: Undeclared colors FD&C Yellow #6, and FD&C Red 40.
Details
Source
Food Recall
External ID
H-0363-2026
Action Date
2026-01-14
Status
Terminated
Category
food
Product Description
Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 oz (226.8 g) boxes, 6/8oz boxes per case. UPC 072981005121 Tita Crackers Rovira, Net Wt. 24 oz (680 g) boxes, 6/24 oz boxes per case. UPC 072981005343 Tita Crackers Rovira, Net Wt 24 oz (680 g) cans, 6/24 oz boxes per case.
Lot/Code Info: Lot numbers: 6/8oz 13125 21025 22425 31725 42125 42926 51925 61625 62325 70125 71425 72225 81125 90225 92225 100725 101424 110625 112224 Lot numbers: 6/24oz 13125 21025 22425 31725 42125 42926 51925 61625 62325 71425 72225 81125 90225 92225 100725 101424 110625 112224 120825 Lot number: 420/24 oz cans 110625
Quantity Affected: 29,246 units
Reason for Recall
Undeclared colors FD&C Yellow #6, and FD&C Red 40
Distribution
GA, TX, MA, IL, MD, USVI and Puerto Rico. Foreign Panama and BVI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-17
Company
Ponce, PR
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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Rovira Biscuit Corporation has 6 FDA actions in our database, including 6 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 (Rovira Biscuit Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Rovira Biscuit Corporation have FDA actions?
Rovira Biscuit Corporation has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0363-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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