Grace Imports, Inc Recall: Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.

🇺🇸 United States

1. August 29, 2024 - Recall initiated
2. October 9, 2024 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0002-2025

Event ID

95311

Status

Ongoing

Classification

Class II

Company

Grace Imports, Inc

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

Quantity

3 cs/30/300 g bags

Reason

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

Recall initiation date

August 29, 2024

Report date

October 9, 2024

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Product were shipped to retail stores in Georgia

UPC, lot, and code information

BATCH NO 2A1564 USE BY 07/30/2025

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 95311 with 2 other product entries in Public Health Trace.

Responsible company: Grace Imports, Inc

Other recalls from Grace Imports, Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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