Rocky Road Ice Cream packaged in a Breyer Chocolate Truffle Tub that says "may contain tree nuts" with a Breyers Rocky R
Summary
The FDA issued a Class II for Rocky Road Ice Cream packaged in a Breyer Chocolate Truffle Tub that says "may c by Unilever Manufacturing (US), Inc.. Reason: Undeclared allergens and mislabeled product. Rocky Road Ice was packaged with Chocolate Truffle Ice Cream labeled tub and a Rocky Road Ice Cream lid..
Details
Source
Food Recall
External ID
H-0017-2025
Action Date
2025-06-18
Status
Terminated
Category
food
Product Description
Rocky Road Ice Cream packaged in a Breyer Chocolate Truffle Tub that says "may contain tree nuts" with a Breyers Rocky Road Ice Cream Lid that declares almonds as an ingredient. 1.5 qt
Lot/Code Info: Lot: JUL1026GB3UPC 077567457288
Quantity Affected: 6668 cases (roughly 12 individual units believed to be affected)
Reason for Recall
Undeclared allergens and mislabeled product. Rocky Road Ice was packaged with Chocolate Truffle Ice Cream labeled tub and a Rocky Road Ice Cream lid. Tub said "may contain tree nuts" the lid said it did contain almonds.
Distribution
Distribution centers and retail locations across the U.S.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-02
Company
Sikeston, MO
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 161 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Unilever Manufacturing (US), Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Unilever Manufacturing (US), Inc. have FDA actions?
This is the only FDA action we have on record for Unilever Manufacturing (US), Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0017-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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