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Lower risk Food recall · FDA · Published October 7, 2016

Le Petit Belge Mini Pancakes Recall: Undeclared Milk in Product

Le Petit Belge recalls Belgian Boys Mini Pancakes (UPC 857290005204) due to undeclared milk. Consumers should check if they own this specific lot and contact the company for details.

🇺🇸 FDA recall #F-0310-2017FoodLe Petit Belge ›
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Contact the company

Recalling firmLe Petit Belge1311 E 34th St · Brooklyn, NY 11210-4819
✎ GovInfoNow plain-language explainer

What happened, in plain English

Le Petit Belge is recalling Belgian Boys Mini Pancakes because they contain undeclared milk. This affects people with milk allergies who might experience allergic reactions. The recall is limited to a specific lot number and UPC. Read more at govinfonow.com/recall/23062-le-petit-belge-mini-pancakes-recall-undeclared-milk-in-product.

Source Summary by GovInfoNow · govinfonow.com/recall/23062-le-petit-belge-mini-pancakes-recall-undeclared-milk-in-product · Updated October 9, 2026 · FDA enforcement record: FDA #F-0310-2017

Cite this page

“Le Petit Belge Mini Pancakes Recall: Undeclared Milk in Product.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23062-le-petit-belge-mini-pancakes-recall-undeclared-milk-in-product. Based on FDA recall #F-0310-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0310-2017%22&limit=1).

Why it’s dangerous

The product contains undeclared milk, meaning it may cause allergic reactions in individuals who are sensitive to milk. This is a food safety issue that requires consumers to check if they have the specific lot number and UPC.

Who’s affected

People with milk allergies are at risk of allergic reactions if they consume the recalled pancakes. The recall applies to specific lots produced in the Netherlands with a best before date of July 7, 2017.

How to tell if you have this one

Check for the UPC 857290005204 on the packaging. The product was produced in the Netherlands and has a best before date of July 7, 2017. The lot number is 20432.

  • Brand
    Le Petit Belge
  • Product
    BELGIAN BOYS MINI PANCAKES, NET WT. 10.6 oz (300g), 36 Count, UPC 857290005204, Product of The Netherlands --- Produced
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 857290005204 and lot number 20432 on the packaging to confirm if the product is recalled.

Where it went and when

Where it was distributed

Distributed in 4 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “Texas, Maryland, California, Illinois, and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Illinois, Maryland, Texas.

Recall timeline

FDA terminated this recall 20 months after the firm started it.

1. Firm started the recall: Oct 7, 201612. FDA classified it Class I: Oct 28, 201623. Published in FDA’s Enforcement Report: Nov 9, 201634. FDA terminated the recall: Jun 19, 2018420162018
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury from this product?

No, the recall is due to a potential allergic reaction, not a physical hazard like choking or fire.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0310-2017 (October 7, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0310-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA