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Lower risk Food recall · FDA · Published April 14, 2026

Lactalis Canada Vanilla Creme Brulee Recall: Glass Foreign Objects Hazard

Lactalis Canada recalls Vanilla Creme Brulee (3.6oz) due to potential glass contamination. Consumers should check product details and contact retailers for returns.

🇺🇸 FDA recall #H-0680-2026FoodLactalis Canada ›
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Recalling firmLACTALIS CANADA, INC405 The West Mall · Toronto, Quebec, Canada
✎ GovInfoNow plain-language explainer

Lactalis Canada is recalling Vanilla Creme Brulee products that may contain glass. This hazard could cause injury if the glass is ingested during consumption. Read more at govinfonow.com/recall/6551-lactalis-canada-vanilla-creme-brulee-recall-glass-foreign-objects-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/6551-lactalis-canada-vanilla-creme-brulee-recall-glass-foreign-objects-hazard · Updated August 10, 2026 · Official notice: FDA #H-0680-2026

Cite this page

“Lactalis Canada Vanilla Creme Brulee Recall: Glass Foreign Objects Hazard.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/6551-lactalis-canada-vanilla-creme-brulee-recall-glass-foreign-objects-hazard. Based on FDA recall #H-0680-2026.

Lactalis Canada, Inc. recalled Specially SELECTED brand Vanilla Creme Brulee products due to the potential presence of glass foreign objects, according to the Food and Drug Administration (FDA). The FDA announced the recall on April 14, 2026.

How to tell if you have it

  • Specially SELECTED brand Vanilla Creme Brulee
  • NET WT 3.6oz (103g)
  • Product Number: 710298-4099100342826
  • Barcode: 4099100342826
  • Best Before/Use By Date: 5/9/2026

The hazard

The product may contain foreign objects, specifically glass. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include JFE Dumpling Party Trays Recall (2026-03-05), Alain Milliat Orange Marmalade Recall (2026-03-26), and Dreyer's Grand Outshine Fruit Bars Grape Recall (2026-08-18).

How to tell if you have this one

Look for the product name 'Specially SELECTED brand Vanilla Creme Brulee' with a net weight of 3.6oz (103g). It was sold exclusively by Aldi Batavia in Canada and packaged in glass jars.

  • Brand
    Lactalis Canada
  • Product
    Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK MIX
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the product name, net weight, and packaging to confirm it matches the recalled items.

Where it went and when

Where it was distributed

Distributed in 7 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: 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: not listedTXFlorida: yesFL

FDA distribution: “NY, IN, FL, IL, VA, MD, and MI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Illinois, Indiana, Maryland, Michigan, New York, Virginia.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Apr 14, 202612. FDA classified it Class II: Apr 28, 202623. Published in FDA’s Enforcement Report: May 6, 202634. FDA terminated the recall: Jul 9, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  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.

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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 #H-0680-2026 (April 14, 2026)
  • Plain-language summary written by qwen3:4b on August 10, 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