“Mondelez Ritz Peanut Butter Cracker Sandwiches Recall: Undeclared Peanuts.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6928-mondelez-ritz-peanut-butter-cracker-sandwiches-recall-undeclared-peanuts. Based on FDA recall #H-0329-2026.
Mondelez Global Llc voluntarily recalled Ritz Peanut Butter Cracker Sandwiches due to undeclared peanut allergens, the FDA said on Nov. 28, 2025. The Class II recall involves 70 cases distributed in Alabama, Georgia, New Jersey, Pennsylvania, New York, Oklahoma, Arkansas, and Missouri.
How to tell if you have it
Brand: Mondelez
Product: Ritz Peanut Butter Cracker Sandwiches, Net Wt. 27.6 oz.- 20 Count (20 x 1.38-oz. 6-pack carton)
Lot Codes: 44000 07584 2
Quantity: 70 cases
The hazard
The product contains undeclared peanuts due to mispackaging, posing an allergy risk to consumers. The FDA classification is Class II.
Context
GovInfoNow's records show Mondelez Global Llc has 9 other recalls on record since Aug. 27, 2014. Other recent recalls of similar products include Mondelez Recalls Baked Bites Brookie Chips Due to Hard Corn Starch Lumps (Dec. 30, 2025), Mondelez Ritz Peanut Butter Cracker Sandwiches Recall: Undeclared Peanuts (July 8, 2025), and Mondelez Recalls BelVita Breakfast Sandwiches with Undeclared Peanuts (July 3, 2023). Other recent recalls of similar products include Mercer's Ice Cream Sandwiches Recall: Undeclared Peanuts in Product (Aug. 25, 2026), Karns Mini Dark Chocolate Raspberry Cups Recall: Undeclared Peanuts Hazard (Jan. 30, 2026), and Jody's Sea Salt Caramel Cheddar Popcorn Recall: Undeclared Peanuts (Oct. 17, 2025).
How to tell if you have this one
Check for the product name 'Ritz Peanut Butter Cracker Sandwiches' and lot code 44000 07584 2 on the packaging. The product was sold in 20-count cartons with a net weight of 27.6 oz.
Brand
Mondelez
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the lot code 44000 07584 2 on the packaging of Ritz Peanut Butter Cracker Sandwiches.
Where it went and when
Where it was distributed
Distributed in 8 states.
Listed by the agency
Not listed
FDA distribution: “The recalled product was distributed to the folowing states: AL, GA, NJ, PA, NY, OK, AR, MO” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, Georgia, Missouri, New Jersey, New York, Oklahoma, Pennsylvania.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0329-2026 (November 28, 2025)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.