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Kettle Cuisine, LLC Recall: Soup labeled Creamy Cauliflower Parmesan Soup may contain undeclared fish and wheat

United States

TerminatedClass I

Company
Kettle Cuisine, LLC
Product
Marketside Creamy Cauliflower Parmesan Soup 16 ounce UPC C…
Recall date
November 11, 2019
Terminated
April 29, 2020
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Marketside Creamy Cauliflower Parmesan Soup 16 ounce UPC Codes: 8113130606 Use By 11/23 through Use by 1/1/20 Not published in this source record 25,772 cases (154,632 cups) Use By 11/23 through Use by 1/1/20 UPC Codes: 8113130606

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0409-2020
Event ID
84250
Status
Terminated
Classification
Class I
Company
Kettle Cuisine, LLC
Product description
Marketside Creamy Cauliflower Parmesan Soup 16 ounce UPC Codes: 8113130606 Use By 11/23 through Use by 1/1/20
Quantity
25,772 cases (154,632 cups)
Reason
Soup labeled Creamy Cauliflower Parmesan Soup may contain undeclared fish and wheat
Recall initiation date
November 11, 2019
Report date
December 11, 2019
Classification date
Not published in this source record
Termination date
April 29, 2020
Distribution pattern
Nationwide
UPC, lot, and code information
Use By 11/23 through Use by 1/1/20 UPC Codes: 8113130606
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Kettle Cuisine, LLC

Other recalls from Kettle Cuisine, LLC

FDA Recall United States Ongoing2026 recordClass I

Kettle Cuisine, LLC

Product
Individual Unit Label (both lid and front of cup): Whole Foo…
Published
June 17, 2026
Distribution
Multiple states

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.