Class ITerminatedVoluntary: Firm initiated
MOMO TEA INC: food recall F-0732-2025
MOMO TEA INC of Maspeth, NY recalled MO-CHA brand Premium Non-Dairy Creamer; INGREDIENTS Glucose syrup, Refined vegetable oil, Whey powder, Sugar, Casein,… Reason: Product does not declare the allergen, milk, on the label. The FDA listed it as Class I in its Enforcement Report dated Apr 30, 2025; distribution: Connecticut, New Jersey, New York.
Record status as published: Terminated (terminated Aug 5, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- MO-CHA brand Premium Non-Dairy Creamer; INGREDIENTS Glucose syrup, Refined vegetable oil, Whey powder, Sugar, Casein, Emulsifier (471, 481i), Stabilizer(340ii, 452i), Anti-caking agent(551), Food flavor; Shelf Life: 24 months; Net Weight (NET WT): 2.2 lbs (1kg); IMPORTED BY Momo Tea Inc.; PRODUCT OF CHINA
- Product quantity
- Approximately 4,500 cases
- Reason for recall
- Product does not declare the allergen, milk, on the label.
- Codes, lots and dates on the package
- No coding. All product on the market is affected.
- Distribution pattern
- NY, NJ, CT
- Recalling firm
- MOMO TEA INC, Maspeth, NY
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 10, 2025 |
| Classified by the FDA | Apr 22, 2025 |
| Published in the Enforcement Report | Apr 30, 2025 |
| Terminated | Aug 5, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0732-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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