Tita Crackers Rovira recall

Recalled by Rovira Biscuit Corporation · Ponce, PR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared colors FD&C Yellow #6, and FD&C Red 40

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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.

Quantity: 29,246 units

Food: Chips & snacks

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Georgia Illinois Massachusetts Maryland Puerto Rico Texas

FDA's distribution note: GA, TX, MA, IL, MD, USVI and Puerto Rico. Foreign Panama and BVI

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Rovira Biscuit Corporation
Initiated by: Voluntary: Firm initiated
Recall initiated: Dec 17, 2025
In FDA report of: Jan 14, 2026
Terminated: Apr 7, 2026
FDA recall number: H-0363-2026 · event 98174
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Labeling Dec 17, 2025