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FDA Recalls International Delight Coffee Creamer, Elevating to Class II Risk
The FDA has recalled more than 75,000 bottles of International Delight coffee creamer across over 30 states due to spoilage ...
FDA recall: 2 popular coffee creamers sold in Mississippi are making people sick. Did you buy?
International Delight coffee creamer sold in Mississippi now under FDA recall. Did you buy them? Are they in your home? What ...
International Delight Coffee Creamer Recalled Over Spoilage Concerns, Per FDA
The U.S. Food and Drug Administration (FDA) announced the recall of more than 75,000 bottles of popular coffee creamers by ...
FDA: International Delight recalling more than 75,000 bottles of coffee creamers in over 30 ...
The U.S. Food and Drug Administration has recalled over 75 thousand bottles of International Delight coffee creamer. Stores ...
FingerLakes1.com7 天
FDA issues Class II recall for International Delight coffee creamers
The Food and Drug Administration has issued a Class II recall for certain International Delight coffee creamers after reports ...
USA Today10 天
More than 75K bottles of popular coffee creamer recalled: See brand, flavors
It was not immediately known how many people became sick. According to the FDA, the recall involves two flavors of International Delight creamer and was initiated on Feb. 21. "International ...
There's a Class II Recall on More Than 75,000 Bottles of International Delight Coffee ...
International Delight is recalling two popular coffee creamers—Cinnabon Classic Cinnamon Roll and Hazelnut—after reports of ...
75,000 bottles of coffee creamer recalled by FDA in Ohio, US. See the full list
More than 75,000 bottles of International Delight coffee creamer are being recalled over concerns the product is spoiled.
Austin American-Statesman10 天
FDA recall: 2 popular coffee creamers sold in Mississippi are making people sick. Did you buy?
According to information from the U.S. Food and Drug Administration, the two flavors of International Delight were sold in more than 30 states. The FDA report says the voluntary recall was ...