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Recall Issued For 75,000 Bottles Of Popular Creamer Due To Health Hazards

A popular coffee creamer has been recalled due to potential health risks, affecting thousands of bottles distributed across 31 states.

Cup of coffee

Cup of coffee

Photo Credit: Pixabay/Myriams-Fotos

International Delight has voluntarily recalled over 75,000 bottles of its coffee creamer after reports of spoilage and illness from consumers, according to the US Food and Drug Administration (FDA).

The recall, initiated on Friday, Feb. 21, was classified as Class II by the FDA on Wednesday, March 12 — indicating that while health risks are not life-threatening, they could cause temporary or medically reversible issues.

The recall affects two flavors of International Delight creamer, manufactured by Danone Wave, based in Louisville, Colorado.

Recalled Products:

Consumers should check their refrigerators for the following products:

Cinnabon Classic Cinnamon Roll International Delight Coffee Creamer

UPC: 0 41271 01993 3

Best By Date: July 3, 2025

Hazelnut International Delight Coffee Creamer

UPC: 0 41271 02565 2

Best By Date: July 2, 2025

The FDA noted that complaints of spoilage and illness led to the recall, though the number of affected customers has not been disclosed.

Where Products Were Sold:

The recalled creamers were shipped to 31 states:

  • Alabama
  • Arkansas
  • Colorado
  • Connecticut
  • Florida
  • Georgia
  • Illinois
  • Indiana
  • Kentucky
  • Louisiana
  • Maryland
  • Maine
  • Michigan
  • Minnesota
  • Missouri
  • Mississippi
  • North Carolina
  • Nebraska
  • New Hampshire
  • New Jersey
  • New Mexico
  • New York
  • Ohio
  • Oklahoma
  • Pennsylvania
  • South Carolina
  • Tennessee
  • Texas
  • Virginia
  • Wisconsin
  • Wyoming

What To Do If You Have Recalled Creamer:

Consumers who have purchased the affected products are advised to check the UPC and Best By Date before consuming. 

Those experiencing symptoms commonly associated with spoiled dairy products —such as nausea, diarrhea, or vomiting — should seek medical attention immediately.

For more details, visit the FDA recall database here.

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