CLASS I Food recall · Reported 11 Dec 2019 · FDA Enforcement Report

Marketside Creamy Cauliflower Parmesan Soup recalled by Kettle Cuisine

Kettle Cuisine is recalling Marketside Creamy Cauliflower Parmesan Soup, distributed nationwide in the US. The recall was initiated on 11 Nov 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUse By 11/23 through Use by 1/1/20 UPC Codes: 8113130606
Quantity recalled25,772 cases (154,632 cups)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0409-2020
FDA event ID
84250
Recalling firm
Kettle Cuisine, Lynn, MA
Classification
Class I
Status
Terminated
Recall initiated
11 Nov 2019
FDA classified
20 Dec 2019
Reported
11 Dec 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Product category
Soup

Timeline

11 Nov 2019Recall initiated by company
11 Dec 2019Published in enforcement report+30 days
20 Dec 2019Classified by FDA+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Soup labeled Creamy Cauliflower Parmesan Soup may contain undeclared fish and wheat

Product as listed by the FDA

Marketside Creamy Cauliflower Parmesan Soup 16 ounce UPC Codes: 8113130606 Use By 11/23 through Use by 1/1/20

Where it was distributed

Nationwide

Nationwide

Stores named: Walmart

Questions about this recall

Why was it recalled?

Soup labeled Creamy Cauliflower Parmesan Soup may contain undeclared fish and wheat

Which lots are affected?

Use By 11/23 through Use by 1/1/20 UPC Codes: 8113130606

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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