Cuisine, Kettle Marketside Tomato Bisque Soup Kit Recall

Why it was recalled

Product had a presumptive positive test result for Listeria monocytogenes

Product description

Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14 OZ (397g), with UPC 1 94346474004. Must Keep Refrigerated.

Lot numbers, UPCs & expiration codes

Best By/ Use By: 8/22/2026

Where it was sold

The recalled product was distributed to the following States: IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, and AR.

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: H-1271-2026
Classification: Class II
Status: Ongoing
Recall initiated: Aug 11, 2026
FDA report date: Sep 2, 2026
Quantity: 540 cases
Recall type: Voluntary: Firm initiated
Recalling firm: CUISINE, KETTLE

Original FDA data

Every field from FDA enforcement report H-1271-2026, exactly as published.

Show all FDA fields

City: Savage
State: MD
Status: Ongoing
Country: United States
Event ID: 99690
Address: 8704 Bollman Pl
Code information: Best By/ Use By: 8/22/2026
Postal code: 20763-9747
Report date: Sep 2, 2026
Product type: Food
Recall number: H-1271-2026
Classification: Class II
Recalling firm: CUISINE, KETTLE
Product quantity: 540 cases
Reason for recall: Product had a presumptive positive test result for Listeria monocytogenes
Voluntary / mandated: Voluntary: Firm initiated
Product description: Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14 OZ (397g), with UPC 1 94346474004. Must Keep Refrigerated.
Distribution pattern: The recalled product was distributed to the following States: IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, and AR.
Recall initiation date: Aug 11, 2026
Initial firm notification: E-Mail
Center classification date: Aug 26, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-1271-2026, published Sep 2, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 7, 2026. Content last changed: Oct 2, 2026.

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