FirstAlerts

FDA Closes Recall of Marketside Tomato Bisque Soup Kit Over Listeria Risk

The FDA has closed the recall of Marketside Tomato Bisque Soup Kit, originally initiated in August 2026 due to a presumptive positive test for Listeria monocytogenes.

2 reports on this incident · first at Sep 7, 2026, 7:12 p.m. ET

By AI ReporterWritten Sep 7, 2026, 7:23 p.m. ET
The U.S. Food and Drug Administration has closed the recall of Marketside Tomato Bisque Soup Kit, recall number , according to an FDA enforcement report dated September 2, 2026. The agency considers the recall carried out. The product, 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, was recalled because it had a presumptive positive test result for Listeria monocytogenes. The recall was initiated on August 11, 2026, and affected distributed to IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, and AR. The product has a Best By/Use By date of 8/22/2026. The FDA classifies this as a recall, meaning the product may cause temporary or medically reversible harm, and the chance of serious harm is remote. Listeria monocytogenes can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems, and infection in pregnant women can cause miscarriage and stillbirth, according to the FDA. Consumers who still have the product with the identifying codes above should not consume it. The FDA database records no other enforcement action by this firm.

Earlier reports

  1. Sep 7, 2026, 7:12 p.m. ETFirst report

    Marketside Tomato Bisque Soup Kit Recalled Over Listeria Risk

    The U.S. Food and Drug Administration (FDA) announced a recall on September 2, 2026, for the Marketside Tomato Bisque Soup Kit, which contains tomato bisque with cheese croutons and white cheddar cheese. The recall, listed as number H-1271-2026, was initiated on August 11, 2026, and is ongoing. The product has a Best By/Use By date of 8/22/2026 and UPC 1 94346474004. Approximately 540 cases are affected, according to the FDA enforcement report.

    The recall was issued because the product had a presumptive positive test result for Listeria monocytogenes. The FDA classifies this as a Class II recall, meaning the product may cause temporary or medically reversible harm, with the chance of serious harm remote. The FDA notes that Listeria monocytogenes can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems, and can cause miscarriage and stillbirth in pregnant women.

    The product was distributed to Illinois, Nevada, New Mexico, California, Oklahoma, Texas, Pennsylvania, Ohio, North Carolina, New York, Georgia, and Arkansas. The recalling firm is Cuisine, Kettle, based in Savage, Maryland. The FDA's database records no other enforcement actions by this firm. The total volume is approximately 7,600 ounces, calculated from the unit count and pack size.

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Revision history

  1. Version 17 Sept 2026, 23:12current

    First published.

  2. Version 17 Sept 2026, 23:23current

    First published.

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