Hometown Food Martha White Gluten Free Sweet Yellow Recall

Why it was recalled

Product tested positive for gluten but is labeled as Gluten free

Product description

Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case. Item UPC: 0 1330082014 8.

Lot numbers, UPCs & expiration codes

Lot codes 9 204 and 9 205. Best if Used by Dates JAN 23 2021 and JAN 24 2021.

Where it was sold

Distribution centers in the following states for two nationwide retailers: CO FL GA NC NJ OH TN VA WI

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-2121-2019
Classification: Class II
Status: Terminated
Recall initiated: Aug 26, 2019
FDA report date: Sep 18, 2019
Quantity: 374 cases
Recall type: Voluntary: Firm initiated
Recalling firm: Hometown Food Company

Original FDA data

Every field from FDA enforcement report F-2121-2019, exactly as published.

Show all FDA fields

City: Chicago
State: IL
Status: Terminated
Country: United States
Event ID: 83639
Address: 500 W Madison St Ste 3650
Code information: Lot codes 9 204 and 9 205. Best if Used by Dates JAN 23 2021 and JAN 24 2021.
Postal code: 60661-4544
Report date: Sep 18, 2019
Product type: Food
Recall number: F-2121-2019
Classification: Class II
Recalling firm: Hometown Food Company
Product quantity: 374 cases
Termination date: Apr 30, 2020
Reason for recall: Product tested positive for gluten but is labeled as Gluten free
Voluntary / mandated: Voluntary: Firm initiated
Product description: Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case. Item UPC: 0 1330082014 8.
Distribution pattern: Distribution centers in the following states for two nationwide retailers: CO FL GA NC NJ OH TN VA WI
Recall initiation date: Aug 26, 2019
Initial firm notification: E-Mail
Center classification date: Sep 9, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2121-2019, published Sep 18, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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