Marketside Tomato Bisque Soup Kit
Marketside Tomato Bisque Soup Kit may be contaminated with Listeria, which can cause serious infections.
Moderate risk
Eating it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Kettle Cuisine LLC of Savage, Maryland recalled Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14 OZ (397g), because the product had a presumptive positive test result for Listeria monocytogenes. The organism can cause serious and sometimes fatal infections in young children, frail or elderly people, and others. The company began the recall on August 11, 2026, and announced it on August 12, 2026.
The recalled product was distributed to Illinois, Nevada, New Mexico, California, Oklahoma, Texas, Pennsylvania, Ohio, North Carolina, New York, Georgia, and Arkansas. Kettle Cuisine LLC recalled 540 cases.
Summary by Recall Canary from the FDA notice.
What to do
If a code on your package matches:
- Consumers who have eaten the recalled product and develop symptoms of listeriosis should contact a healthcare provider.
- Pregnant people should contact a healthcare provider promptly if they experience fever or other symptoms after possible exposure.
- Consumers/Media with questions may contact Kettle Cuisine Hotline at 617-409-1104 Monday to Friday, 8am thru 5pm ET.
- Do not eat, serve, sell, or distribute the recalled product. Dispose of the product or return it to the place of purchase for a refund. Do not rely on smell or appearance to determine whether the product is safe.
Is your kit affected?
Match the best-by date and UPC listed under your product.
Tomato Bisque Soup Kit
- Size
- 14 oz (397g)
- UPC
- 194346474004
- Best-by
- 8/22/26
- Brand
- Marketside
- Quantity recalled
- 3240 packs
Details
- Company began the recall
- Sold in
- 12 states
- Event ID
- 99690
- Recall No.
- H-1271-2026
- Company
- CUISINE, KETTLESavage, Maryland
- Hazard
- Listeria
- Quantity recalled
- 540 cases
- Recall type
- Voluntary: Firm initiated
- Customers told by
Company began the recall
Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Summary updated
