RecallRadar
ModerateReported December 31, 2025

Ritz Peanut Butter Cracker Sandwiches

Recalled by Mondelez Global Llc

Food recall

Mondelez Global Llc

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 an undeclared allergen

Mondelez Global Llc has recalled Ritz Peanut Butter Cracker Sandwiches, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 31, 2025 and was initiated on November 28, 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 Ritz Peanut Butter Cracker Sandwiches, with approximately 70 cases affected. The company behind the recall is Mondelez Global Llc, based in East Hanover, NJ. The FDA describes the product as: “Ritz Peanut Butter Cracker Sandwiches, Net Wt. 27.6 oz.- 20 Count (20 x 1.38-oz. 6-pack carton)”

Why was Ritz Peanut Butter Cracker Sandwiches recalled?

According to the FDA, the stated reason for the recall is: “Undeclared allergens (Peanut) due to mispackaging.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought Ritz Peanut Butter Cracker Sandwiches, compare it against the product description and identifying codes (Lot Codes: 44000 07584 2) 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 Mondelez Global Llc or your local health authority.

About this recall

This recall was distributed in NJ. 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
December 31, 2025
Recall started
November 28, 2025
Distributed in
NJ
What was recalled
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 27.6 oz.- 20 Count (20 x 1.38-oz. 6-pack carton)
Why it was recalled (as stated by the FDA)
Undeclared allergens (Peanut) due to mispackaging
How to identify the affected product
Lot Codes: 44000 07584 2
Amount recalled
70 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 Ritz Peanut Butter Cracker Sandwiches recalled?+

According to the FDA: Undeclared allergens (Peanut) due to mispackaging

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 Ritz Peanut Butter Cracker Sandwiches?+

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-0329-2026. Information last synced from the FDA on July 6, 2026.

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