RecallRadar
ModerateReported November 5, 2025

Marketside Cheesy Cauliflower Au Gratin 12 oz.

Recalled by FreshRealm, Inc

Food recall

FreshRealm, Inc

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

See all recalls involving Listeria

FreshRealm, Inc has recalled Marketside Cheesy Cauliflower Au Gratin 12 oz., according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 5, 2025 and was initiated on September 27, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Marketside Cheesy Cauliflower Au Gratin 12 oz., with approximately 3,428 units affected. The company behind the recall is FreshRealm, Inc, based in Indianapolis, IN. The FDA describes the product as: “Marketside Cheesy Cauliflower Au Gratin 12 oz.; UPC: 10194346375445”

Why was Marketside Cheesy Cauliflower Au Gratin 12 oz. recalled?

According to the FDA, the stated reason for the recall is: “Potential contamination with listeria monocytogenes.” In plain terms, this recall relates to Listeria.

Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.

What should you do?

If you think you may have bought Marketside Cheesy Cauliflower Au Gratin 12 oz., compare it against the product description and identifying codes (Best if used by Dates: 9/23/2025 through 10/04/2025 (production dates 9/11, 9/15, 9/18, 9/22)) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact FreshRealm, Inc or your local health authority.

About this recall

This recall was distributed in IN. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
November 5, 2025
Recall started
September 27, 2025
Distributed in
IN
What was recalled
Marketside Cheesy Cauliflower Au Gratin 12 oz.; UPC: 10194346375445
Why it was recalled (as stated by the FDA)
Potential contamination with listeria monocytogenes
How to identify the affected product
Best if used by Dates: 9/23/2025 through 10/04/2025 (production dates 9/11, 9/15, 9/18, 9/22)
Amount recalled
3,428 units

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Marketside Cheesy Cauliflower Au Gratin 12 oz. recalled?+

According to the FDA: Potential contamination with listeria monocytogenes

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Marketside Cheesy Cauliflower Au Gratin 12 oz.?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0141-2026. Information last synced from the FDA on July 6, 2026.

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