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Le Petit Belge Recall: The product/lot contains undeclared milk.

United States

TerminatedClass I

Company
Le Petit Belge
Product
BELGIAN BOYS MINI PANCAKES, NET WT. 10.6 oz (300g), 36 Count…
Recall date
October 7, 2016
Terminated
June 19, 2018
Source
FDA

Reason for recall

The product/lot contains undeclared milk.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
BELGIAN BOYS MINI PANCAKES, NET WT. 10.6 oz (300g), 36 Count, UPC 857290005204, Product of The Netherlands --- Produced exclusively for Belgian Boys, 140 Carolyn Blvd., Farmingdale, NY 11735 857290005204 US: 240 cases (12 units per case); Canada: 240 cases (12 units per case) Lot 20432, Best Before Jul 07 2017

Distribution

  • Texas
  • Maryland
  • California
  • Illinois
  • and Canada

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0310-2017
Event ID
75397
Status
Terminated
Classification
Class I
Company
Le Petit Belge
Product description
BELGIAN BOYS MINI PANCAKES, NET WT. 10.6 oz (300g), 36 Count, UPC 857290005204, Product of The Netherlands --- Produced exclusively for Belgian Boys, 140 Carolyn Blvd., Farmingdale, NY 11735
Quantity
US: 240 cases (12 units per case); Canada: 240 cases (12 units per case)
Reason
The product/lot contains undeclared milk.
Recall initiation date
October 7, 2016
Report date
November 9, 2016
Classification date
Not published in this source record
Termination date
June 19, 2018
Distribution pattern
Texas, Maryland, California, Illinois, and Canada
UPC, lot, and code information
UPC 857290005204; Lot 20432, Best Before Jul 07 2017
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

Responsible company: Le Petit Belge

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:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.