FDA recall, , Moderate risk
Specially Selected Vanilla Creme Brulee
Vanilla Creme Brulee may contain foreign objects, specifically glass.
Recall ended Jul 9, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
LACTALIS CANADA, INC, of Toronto, Quebec, Canada, recalled Specially SELECTED brand Vanilla Creme Brulee because the product may contain foreign objects, specifically glass. The product, sold exclusively by ALDI in Batavia, IL, in glass jars, was distributed in Florida, Illinois, Indiana, Maryland, Michigan, New York and Virginia. The company began the recall on April 14, 2026, and the FDA added it to the Enforcement Report on April 28, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
A UPC is the number printed under a barcode.
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
- UPC
- 4099100342826
Recall details
- Company began the recall
- Company
- LACTALIS CANADA, INCToronto, Quebec, Canada
- Hazard
- Foreign object
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98771
- Recall number
- H-0680-2026
- Quantity recalled
- 2,869 cases
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Recall ended
Archived
Summary updated
