RecallRadar
ModerateReported April 1, 2026

14" Margarita Thin Crust Pizza

Recalled by Rose and Shore, Inc.

Food recall

Rose and Shore, 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 foreign material

Rose and Shore, Inc. has recalled 14" Margarita Thin Crust Pizza, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 1, 2026 and was initiated on January 14, 2026. 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 14" Margarita Thin Crust Pizza, with approximately 5,067.1 cases affected. The company behind the recall is Rose and Shore, Inc., based in Vernon, CA. The FDA describes the product as: “14" Margarita Thin Crust Pizza; 8 units per case. Keep Frozen UPC code: 1713940060”

Why was 14" Margarita Thin Crust Pizza recalled?

According to the FDA, the stated reason for the recall is: “potential foreign object (metal pieces) in ingredient (Tomatoes).” In plain terms, this recall relates to foreign material.

A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.

What should you do?

If you think you may have bought 14" Margarita Thin Crust Pizza, compare it against the product description and identifying codes (Lots 12255, 22265, 12415.) before using it. This recall is currently listed as ongoing.

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 Rose and Shore, Inc. or your local health authority.

About this recall

This recall was distributed in CA. 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
Ongoing
Date reported
April 1, 2026
Recall started
January 14, 2026
Distributed in
CA
What was recalled
14" Margarita Thin Crust Pizza; 8 units per case. Keep Frozen UPC code: 1713940060
Why it was recalled (as stated by the FDA)
potential foreign object (metal pieces) in ingredient (Tomatoes)
How to identify the affected product
Lots 12255, 22265, 12415.
Amount recalled
5,067.1 cases

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 14" Margarita Thin Crust Pizza recalled?+

According to the FDA: potential foreign object (metal pieces) in ingredient (Tomatoes)

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 14" Margarita Thin Crust Pizza?+

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-0622-2026. Information last synced from the FDA on July 5, 2026.