Lidl US TRADING Recall: Lidl US has voluntarily recalled all Bellona brand Milk Chocolate Flavored Coated Wafer with Hazelnut Cr¿me Filling and White Chocolate Flavor confections as a precautionary measure because the allergen statement does not include wheat.

🇺🇸 United States

1. September 13, 2018 - Recall initiated
2. October 24, 2018 - Reported by source
3. January 6, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0037-2019

Event ID

81049

Status

Terminated

Classification

Class II

Company

Lidl US TRADING

Product description

Bellona brand Milk Chocolate Flavored Coated Wafer with Hazelnut Cr¿me Filling and White Chocolate Flavor, 5.3 oz. (150g) package containing 7 single-serving, foil-wrapped chocolate wafers on a cardboard tray with foil overwrap.

Quantity

52,000 units have been sold

Reason

Lidl US has voluntarily recalled all Bellona brand Milk Chocolate Flavored Coated Wafer with Hazelnut Cr¿me Filling and White Chocolate Flavor confections as a precautionary measure because the allergen statement does not include wheat.

Recall initiation date

September 13, 2018

Report date

October 24, 2018

Classification date

Not published in this source record

Termination date

January 6, 2021

Distribution pattern

Product was sold at Lidl retail locations in the following states: Virginia, Delaware, New Jersey, Maryland, Georgia, North Carolina, South Carolina.

UPC, lot, and code information

UPC: 20343613

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Lidl US TRADING

Other recalls from Lidl US TRADING

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

• Email
• X / Twitter
• Facebook