NEUHAUS brand ORIGINAL BELGIAN CHOCOLATE; POPPING MILK CHOCOLATES WITH COOKIES; 4.23 oz - 120g; (EN)Chocolates - INGREDI
Summary
The FDA issued a Class I for NEUHAUS brand ORIGINAL BELGIAN CHOCOLATE; POPPING MILK CHOCOLATES WITH COOKIES; by Neuhaus nv. Reason: Product contains undeclared wheat..
Details
Source
Food Recall
External ID
H-0582-2025
Action Date
2025-09-24
Status
Terminated
Category
food
Product Description
NEUHAUS brand ORIGINAL BELGIAN CHOCOLATE; POPPING MILK CHOCOLATES WITH COOKIES; 4.23 oz - 120g; (EN)Chocolates - INGREDIENTS: milk chocolate (sugar, whole milk powder, cocoa mass, cocoa butter, emulsifier: soy lecithin, flavour), sugar, sunflower oil, whole milk powder, cocoa butter, skimmed milk powder, carmelised sugar, cocoa mass, glucose syrup, emulsifier: soy lecithin, spices, lactose, flavours, acidity regululator: malic acid; carbon dioxide. May contain traces of eggs, sesame, groundnuts and nuts
Lot/Code Info: Batch Number: 80108690 with Best before date: 13/01/2026 (DD/MM/YYYY) Batch Number: 80108763 with Best before date: 13/01/2026 (DD/MM/YYYY)
Quantity Affected: 100 pieces
Reason for Recall
Product contains undeclared wheat.
Distribution
VA, MD, PA, NY, and Washington DC
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-04
Company
Vlezenbeek, N/A
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Neuhaus nv) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Neuhaus nv have FDA actions?
This is the only FDA action we have on record for Neuhaus nv in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0582-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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