Class II Recall

KERALA MIXTURE INGREDIENTS: Gram Flour 48%, Edible Veg Oil (Refined Palmolein Oil) 36%, Peanuts 6%, Roasted Bengal Gram,

Summary

The FDA issued a Class II for KERALA MIXTURE INGREDIENTS: Gram Flour 48%, Edible Veg Oil (Refined Palmolein Oi by Grace Imports, Inc. Reason: Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label..

Details

Source

Food Recall

External ID

F-0002-2025

Action Date

2024-10-09

Status

Ongoing

Product Description

KERALA MIXTURE INGREDIENTS: Gram Flour 48%, Edible Veg Oil (Refined Palmolein Oil) 36%, Peanuts 6%, Roasted Bengal Gram, Salt 1.5%, Chilly powder 1%, Curry leaf, Asafoetida, Natural Antioxidant (Mixed Tocopherol INS 305) ALLERGEN INFORMATION: Made in a Factory that Process Peanuts, Tree nuts, Soy, Milk, Wheat Sesame and Jaggery UPC 8 904123 500329 NET QUANTITY 300 g Mfd. by: A1 CHIPS AND EXPORTS INDIA PVT. LTD 346 RDM Chinna Thottam, Pachapalayam, Kalampalayam Colmbatore 641010, Tamil Nadu, India

Lot/Code Info: BATCH NO 2A1564 USE BY 07/30/2025

Quantity Affected: 3 cs/30/300 g bags

Reason for Recall

Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.

Distribution

Product were shipped to retail stores in Georgia

Type: Voluntary: Firm initiated

Recall Initiated: 2024-08-29

Company

Grace Imports, Inc

Tucker, GA

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 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Grace Imports, Inc has 3 FDA actions in our database, including 3 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 (Grace Imports, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Grace Imports, Inc have FDA actions?

Grace Imports, Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0002-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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