Momo Tea Inc food recall: MO-CHA brand Premium Non-Dairy Creamer
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96675
- Recall initiated
- Apr 10, 2025
- Classified by FDA
- Apr 22, 2025
- Posted in Enforcement Report
- Apr 30, 2025
- Terminated
- Aug 5, 2025
- Recalling firm
- MOMO TEA INC
- Firm location
- Maspeth, NY, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product does not declare the allergen, milk, on the label.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Apr 10, 2025. FDA classified it 12 days later, on Apr 22, 2025. Distribution reported by FDA: NY, NJ, CT
Recalled products (1)
F-0732-2025 Class I Terminated
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
Codes / lots: No coding. All product on the market is affected.
Quantity: Approximately 4,500 cases
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 96675
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.