RecallHawk
Class II Recall

Tempting Crackers Tray, Rovira, 3 foil wrap trays per Net Wt. 8oz box (Net Wt 5 oz trays), 6 box per case. UPC 072981003

Rovira Biscuit Corporation

Summary

The FDA issued a Class II for Tempting Crackers Tray, Rovira, 3 foil wrap trays per Net Wt. 8oz box (Net Wt 5 by Rovira Biscuit Corporation. Reason: Undeclared colors FD&C Yellow #6, and FD&C Red 40.

Details

Source

Food Recall

External ID

H-0359-2026

Action Date

2026-01-14

Status

Terminated

Category

food

Product Description

Tempting Crackers Tray, Rovira, 3 foil wrap trays per Net Wt. 8oz box (Net Wt 5 oz trays), 6 box per case. UPC 072981003127 Tempting Crackers, Rovira, 12 packets (Net Wt. 1.0 oz (30 g) bag) per box, 12/ 1.0 oz packets box, 6/ 12-1oz box per case. UPC 072981003127

Lot/Code Info: Lot numbers: 10725 21025 31025 50426 50525 63025 70125 80924 91925 111824

Quantity Affected: 9,838 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

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-0359-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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