Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 o…
Recalled by Rovira Biscuit Corporation

Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Rovira Biscuit Corporation has recalled Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 o…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 14, 2026 and was initiated on December 17, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 o…, with approximately 29,246 units affected. The company behind the recall is Rovira Biscuit Corporation, based in Ponce, PR. The FDA describes the product as: “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)…”
Why was Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 o… recalled?
According to the FDA, the stated reason for the recall is: “Undeclared colors FD&C Yellow #6, and FD&C Red 40.” In plain terms, this recall relates to an undeclared ingredient or allergen.
An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.
What should you do?
If you think you may have bought Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 o…, compare it against the product description and identifying codes (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 13…) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Rovira Biscuit Corporation or your local health authority.
About this recall
This recall was distributed in PR. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Terminated
- Date reported
- January 14, 2026
- Recall started
- December 17, 2025
- Distributed in
- PR
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 o… recalled?+
According to the FDA: Undeclared colors FD&C Yellow #6, and FD&C Red 40
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Tita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 o…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0363-2026. Information last synced from the FDA on July 6, 2026.