“Kettle Cuisine Minestrone Soup Recall: Undeclared Shrimp Allergen.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6213-kettle-cuisine-minestrone-soup-recall-undeclared-shrimp-allergen. Based on FDA recall #H-0941-2026.
Kettle Cuisine, LLC voluntarily recalled Whole Foods Market Kitchens Minestrone Soup after the FDA announced on May 19, 2026, that the product contains undeclared shrimp. The Food and Drug Administration issued recall number H-0941-2026 for the Class I hazard.
How to tell if you have it
Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ
UPC: 099482502065
Lot/Unit Number: 1762181
Use by date: 05/27/26
The hazard
The soup contains undeclared shrimp, an allergen that poses a risk to consumers with shellfish allergies. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show Kettle Cuisine, LLC has two other recalls on record since January 12, 2017, including a 2019-11-11 Marketside Creamy Cauliflower Parmesan Soup recall for undeclared fish and wheat. Other recent recalls of similar products include Rockport Lobser Bisque (2025-10-29), Grandma Belle's Tomato Basil Soup (2025-12-04), and Pacific Seafood Shrimp (2025-11-08).
How to tell if you have this one
Check the product label for the lot number (1762181) or UPC code (09948:2502065). The product is labeled as 'Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ'.
Brand
Kettle Cuisine
Product
Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the lot number (1762181) or UPC code (099482502065) on the label.
Where it went and when
Where it was distributed
Distributed in 17 states and D.C..
Listed by the agency
Not listed
FDA distribution: “AL, CT, DC, FL, GA, MA, MD, ME, MS, NC, NH, NJ, NY, PA, RI, SC, TN, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Connecticut, District of Columbia, Florida, Georgia, Maine, Maryland, Massachusetts, Mississippi, New Hampshire, New Jersey, New York, North Carolina, Pennsylvania, Rhode Island, South Carolina, Tennessee, Virginia.
Recall timeline
FDA published this recall 29 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0941-2026 (May 19, 2026)
Plain-language summary written by qwen3:4b on August 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.