Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese 1.35 oz Packs and 10 Peanut Butter 1.38
Summary
The FDA issued a Class II for Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese by Mondelez Global Llc. Reason: Undeclared allergens (Peanut) due to mispackaging.
Details
Source
Food Recall
External ID
H-0325-2025
Action Date
2025-07-30
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: 2 NOV 25 - 9 NOV 25
Quantity Affected: 13,872 cases
Reason for Recall
Undeclared allergens (Peanut) due to mispackaging
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
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-08
Company
East Hanover, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mondelez Global Llc has 13 FDA actions in our database, including 13 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mondelez Global Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mondelez Global Llc have FDA actions?
Mondelez Global Llc has 13 FDA actions in our database, including 13 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0325-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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