“Marketside Creamy Cauliflower Parmesan Soup Recall: Undeclared Fish and Wheat.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/16267-marketside-creamy-cauliflower-parmesan-soup-recall-undeclared-fish-and-wheat. Based on FDA recall #F-0409-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0409-2020%22&limit=1).
The FDA announced on November 11, 2019, that Kettle Cuisine, LLC voluntarily recalled Marketside Creamy Cauliflower Parmesan Soup due to undeclared fish and wheat allergens. Consumers should check their product labels for the specified use-by dates.
How to tell if you have it
Marketside Creamy Cauliflower Parmesan Soup
16 ounce
UPC 8113130606
Use By 11/23 through Use by 1/1/20
The hazard
The soup may contain undeclared fish and wheat, posing an allergy risk to consumers. 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. Other recent recalls of similar products include Koi Koi Trading Fish Balls Recall (January 28, 2026), Recall: Sliced Korean Halibut with Soy Sauce May Contain Undeclared Allergens (July 1, 2026), and WFM Purchasing Brussel Sprouts & Kale Slaw Recall (December 31, 2025).
How to tell if you have this one
Look for Marketside Creamy Cauliflower Parmesan Soup in 16-ounce containers. Check the UPC code, which is 8113130606. Verify the Use By date falls between 11/23 and 1/1/20.
Brand
Marketside
Product
Marketside Creamy Cauliflower Parmesan Soup 16 ounce UPC Codes: 8113130606 Use By 11/23 through Use by 1/1/20
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop consuming the soup
Do not eat the product if it matches the recalled UPC and date range.
Check your product details
Verify the UPC is 8113130606 and the Use By date is between 11/23 and 1/1/20.
Contact the manufacturer
Reach out to Kettle Cuisine, LLC for further instructions on disposal or refund.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class I
4FDA terminated the recall
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 #F-0409-2020 (November 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0409-2020 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.