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Lower risk Food recall · FDA · Published July 8, 2025

Mondelez Ritz Peanut Butter Cracker Sandwiches Recall: Undeclared Peanuts

Mondelez recalls Ritz Peanut Butter Cracker Sandwiches due to undeclared peanuts in packaging. This poses a risk for people with peanut allergies. Consumers should check for the specific UPC code and recall date range.

🇺🇸 FDA recall #H-0326-2025FoodMondelez ›
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Recalling firmMondelez Global Llc100 Deforest Ave · East Hanover, NJ 07936-2813
✎ GovInfoNow plain-language explainer

What happened, in plain English

Mondelez is recalling Ritz Peanut Butter Cracker Sandwiches because they contain undeclared peanuts, which can cause allergic reactions in people sensitive to peanuts. This recall affects products sold between November 1 and November 9, 2025, with a specific UPC code. Read more at govinfonow.com/recall/7571-mondelez-ritz-peanut-butter-cracker-sandwiches-recall-undeclared-peanuts.

Source Summary by GovInfoNow · govinfonow.com/recall/7571-mondelez-ritz-peanut-butter-cracker-sandwiches-recall-undeclared-peanuts · Updated August 17, 2026 · Official notice: FDA #H-0326-2025

Cite this page

“Mondelez Ritz Peanut Butter Cracker Sandwiches Recall: Undeclared Peanuts.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/7571-mondelez-ritz-peanut-butter-cracker-sandwiches-recall-undeclared-peanuts. Based on FDA recall #H-0326-2025.

Why it’s dangerous

The crackers contain undeclared peanuts, meaning they are packaged without clear labeling of peanut content. This can cause allergic reactions in individuals sensitive to peanuts, especially if they have severe allergies.

Who’s affected

People with peanut allergies are at risk from this recall. The product was sold in specific packaging with a UPC code 0 44000 88210 5 between November 1 and November 9, 2025.

How to tell if you have this one

Check for the UPC code 0 44000 88210 5 on the packaging. The product was sold in cartons labeled '14X8-Case: 14 - 11.04 Oz Cartons in master carton' between November 1 and November 9, 2025.

  • Brand
    Mondelez
  • Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton
  • Category
    Food
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    The recalled product was distributed to the following states: AK,AL,AR,AZ,CA,CO,CT,DC,DE,FL,GA,HI,IA,ID,IL,IN,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,ND,NE,NH,NJ,NM,NV,NY,OH,OK,OR,PA,RI,SC,TN,TX,UT,VA,WA,WI,WV,WY
Recall numberProduct, codes & lotsQuantity
H-0323-2025Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside cartons. And 6x20(6 - 27.6 oz Cartons) in master carton. UPC 1 00 44000 07584 2; 1 NOV 25 - 9 NOV 25 2 JAN 26 - 22 JAN 2624,446 cases
H-0324-2025Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 count (40x1.38 oz 6 pack of cracker sandwiches inside carton. 40 - 55.2oz Cartons in master carton. UPC 0 44000 07819 5; 1 NOV 25 - 9 NOV 25 2 JAN 26 - 22 JAN 26224 cases
H-0325-2025Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese 1.35 oz Packs and 10 Peanut Butter 1.38 oz Packs) Net Wt. 27.3 oz (20-1.38 oz packet of cracker sandwiches inside cartons of varying sizes). 20-27.3 OZ (Case: 6 - 27.3 Oz Cartons in master carton. UPC 0 44000 08095 2; 2 NOV 25 - 9 NOV 2513,872 cases
H-0326-2025Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton. 14X8-Case: 14 - 11.04 Oz Cartons in master carton. UPC 0 44000 88210 5; 1 NOV 25 - 9 NOV 25 "AE" Plant Code Only37,985
Based on the official FDA remedy

What to do — step by step

  1. Check Packaging

    Look for the UPC code 0 44000 88210 5 on the product packaging.

Where it went and when

Where it was distributed

Distributed in 48 states and D.C..

Alaska: yesAKMaine: yesMEVermont: not listedVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “The recalled product was distributed to the following states: AK,AL,AR,AZ,CA,CO,CT,DC,DE,FL,GA,HI,IA,ID,IL,IN,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,ND,NE,NH,NJ,NM,NV,NY,OH,OK,OR,PA,RI,SC,TN,TX,UT,VA,WA,WI,WV,WY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 22 days after the firm started it.

1. Firm started the recall: Jul 8, 202512. FDA classified it Class II: Jul 22, 202523. Published in FDA’s Enforcement Report: Jul 30, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-0326-2025 (July 8, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA