Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK MIX (E
Summary
The FDA issued a Class II for Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: by LACTALIS CANADA, INC. Reason: Product may contain foreign objects, specifically glass..
Details
Source
Food Recall
External ID
H-0680-2026
Action Date
2026-05-06
Status
Completed
Category
food
Product Description
Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK MIX (EGG YOLK, SUGAR) SUGAR, NATURAL VANILLA FLAVOR, TAPIOCA STARCH, CARRAGEENAN; TOPPING INGREDIENTS: CARAMEL FLAKES (SUGAR, GLUCOSE SYRUP); CONTAINS: MILK, EGGS. MAY CONTAIN: WHEAT, SOY; DIST.SOLD EXCLUSIVELY BY: ALDI BATAVIA, IL; packaged in glass jars
Lot/Code Info: Best Before/Use By Date: 5/9/2026 Product Number: 710298-4099100342826 Barcode: 4099100342826
Quantity Affected: 2,869 cases
Reason for Recall
Product may contain foreign objects, specifically glass.
Distribution
NY, IN, FL, IL, VA, MD, and MI
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-14
Company
Toronto, Quebec
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 19 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 (LACTALIS CANADA, INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does LACTALIS CANADA, INC have FDA actions?
This is the only FDA action we have on record for LACTALIS CANADA, INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0680-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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