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Coffee Creamer Recalled as FDA Sets Highest Risk Level

Coffee Creamer Recalled as FDA Sets Highest Risk Level

Newsweek24-04-2025

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources.
Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content.
A nondairy coffee creamer sold across the Northeast has been recalled after it was found that it could pose serious health risks to consumers with milk allergies.
MO-CHA brand Premium Non-Dairy Creamer, imported by Momo Tea Inc. of Maspeth, New York, was voluntarily recalled after it was found to contain undeclared milk ingredients.
On Tuesday, the Food and Drug Administration (FDA) classified the recall as Class I, its most serious designation.
Newsweek has contacted Momo Tea Inc via social media for comment.
Why It Matters
Federal food labeling regulations require that all major allergens, including milk, be clearly disclosed on packaging. The recalled product includes milk-derived ingredients, whey powder and casein, but does not declare milk as an allergen on its label.
This type of labeling omission can be life-threatening for individuals with milk allergies as food allergy symptoms can include hives, rashes, vomiting, diarrhea, stomach cramps, respiratory issues and, in severe cases, anaphylaxis—a condition marked by throat swelling, a drop in blood pressure, difficulty breathing and loss of consciousness.
File photo: milk being poured into a mug of coffee.
File photo: milk being poured into a mug of coffee.
Agencia el Universal/GDA via AP
What To Know
The affected product, which was imported from China and packaged in 2.2-pound bags, has a shelf life of two years.
There are no lot codes or unique identifiers listed in the recall notice. According to the FDA, all units of the product on the market are subject to the recall, with about 4,500 cases distributed across New York, New Jersey and Connecticut.
Momo Tea Inc. initiated the recall on April 10, and the FDA released its classification on April 22.
FDA's classification indicates a reasonable probability that consumption could cause severe health consequences or death, as a Class I recall determines "a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death."
Ingredients listed on the product label include glucose syrup, refined vegetable oil, whey powder, sugar and various food additives.
What People Are Saying
Dr. Sebastian Lighvani, the director of New York Allergy & Asthma PLLC, previously told Newsweek: "Every three minutes in the United States, someone ends up in an emergency room because of an allergic reaction after accidental ingestion of food. So even when we try hard, these reactions are happening. And if you look at the incidence of anaphylaxis, it has skyrocketed in the last 5, 10, 20 years. And in the U.S., there's like a 300 to 400 percent increase in the rates of anaphylaxis to foods."
What Happens Next
According to the FDA's notice, the recall is still ongoing.

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