Warning: Popular Coffee Creamer Recalled in Minnesota Over Spoilage Concerns

One of the best parts of my day is when I grab my cup of fresh coffee, pour some creamer in it to make it perfect, and take that first sip.  Unfortunately, that first sip is tasting like barf for quite a few people in multiple states, including in Minnesota.  It has even been reported that this spoiled coffee creamer is making people sick.

To avoid that nasty first sip, check out the latest recall involving a popular coffee creamer.

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Thousands of Bottles of Coffee Creamer Recalled in Minnesota Due to Spoilage

According to the U.S. Food and Drug Administration, a voluntary recall was issued by the parent company of International Delight.  Based on the data in the enforcement report, the recall is a Class II designation and impacts over 75,000 bottles of coffee creamer in over 31 states.  (Class II designation explained in more detail below.)

What States Are Impacted By The Coffee Creamer Recall?

There are 31 states total that are impacted by the International Delight coffee creamer recall including:

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

What Coffee Creamers Are Part of the International Delight Coffee Creamer Recall?

The latest recall posted on the FDA enforcement report indicated that the following coffee creamers were listed in the recall:

International Delight Cinnabon Classic Cinnamon Roll Coffee Creamer

• 32 oz fluid bottle
• 46,482 bottles recalled
• UPC code 0 41271 01993 3
• Best by date - July 3rd, 2025
• Plant code 51-4114 R-S

International Delight Hazelnut Coffee Creamer

• 32 oz fluid bottle
• 28,572 bottles recalled
• UPC code 0 41271 02565 2
• Best by date - July 2nd, 2025
• Plant code 51-4114 R-S

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What Is An FDA Class II Designation?

Good Morning America reported on the recall as well and indicated that provided more details on the designation of this recall.  Based on their story, a Class II designation indicates that the products recalled "may cause temporary or medically reversible adverse health consequences".  There is a chance of "serious adverse health consequences" but those are lower.

Where You Can Find The List of Additional Recalled Items

The U.S. Food and Drug Administration publishes a list daily with current items that are part of a recall.  This list includes medical devices, drugs, toys, clothing, beverages, food, furniture, and more.

To see the latest items that have been recalled, visit the U.S. Food and Drug Administration website.