Ritz Peanut Butter Cracker Sandwiches and 3 more products

The 4 products

1. Ritz Peanut Butter Cracker Sandwiches

   Ritz 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

   Codes and dates

   1 NOV 25 - 9 NOV 25 2 JAN 26 - 22 JAN 26

   Quantity

   24,446 cases

   Class

   Class II

   Recall number

   H-0323-2025

2. Ritz Peanut Butter Cracker Sandwiches

   Ritz 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

   Codes and dates

   1 NOV 25 - 9 NOV 25 2 JAN 26 - 22 JAN 26

   Quantity

   224 cases

   Class

   Class II

   Recall number

   H-0324-2025

3. Ritz Cracker Sandwiches, Variety

   Ritz 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

   Codes and dates

   2 NOV 25 - 9 NOV 25

   Quantity

   13,872 cases

   Class

   Class II

   Recall number

   H-0325-2025

4. Ritz Peanut Butter Cracker Sandwiches

   Ritz 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

   Codes and dates

   1 NOV 25 - 9 NOV 25 "AE" Plant Code Only

   Quantity

   37,985

   Class

   Class II

   Recall number

   H-0326-2025

Where it was distributed

In FDA’s words:

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

What Class II means

In FDA’s definitions, a Class II recall is one where: use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse health consequences is remote. FDA’s recall definitions

If you have this product

• FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
• FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
• If someone has a serious allergic reaction, call 911. Signs of a serious reaction

Source

FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of July 30, 2025. openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.