RecallHawk
Class III Recall

BarbaCuban Ram Air Red Zesty Ketchup, Net Wt. 12 oz (355 ml) 12 oz glass bottles, and 1 gallon HDPE Industrial Plastic J

Prima Foods International, Inc.

Summary

The FDA issued a Class III for BarbaCuban Ram Air Red Zesty Ketchup, Net Wt. 12 oz (355 ml) 12 oz glass bottles by Prima Foods International, Inc.. Reason: Undeclared Quinine.

Details

Source

Food Recall

External ID

H-0446-2026

Action Date

2026-02-11

Status

Terminated

Category

food

Product Description

BarbaCuban Ram Air Red Zesty Ketchup, Net Wt. 12 oz (355 ml) 12 oz glass bottles, and 1 gallon HDPE Industrial Plastic Jugs, ¿ gallon HDPE Industrial Plastic Jugs. packaged in 12x12 fl oz, 6x12 fl oz, 4x1 gallon, 4x1/2 gallons. UPC code 0 07196 60000 7

Lot/Code Info: Lot Codes: #133/25 Best by dates: 11/2026

Quantity Affected: 12,214 bottles total

Reason for Recall

Undeclared Quinine

Distribution

Distributed in Florida

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-17

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Prima Foods International, Inc. has 6 FDA actions in our database, including 6 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 Foods International, 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 Foods International, Inc. have FDA actions?

Prima Foods International, Inc. 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-0446-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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