Man Fon Wonton Wrappers
Man Fon Wonton Wrappers contain undeclared colors Yellow#5 and Yellow#6.
Recall ended Aug 28, 2026. Still check yours.
Moderate risk
Eating it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Man Fon, Inc. of San Gabriel, California, recalled Won Ton Wrappers Extra Thin and Wonton Wrappers on July 8, 2026, because the products contain undeclared colors Yellow#5 and Yellow#6, and the Wonton Wrappers also lack ingredient labeling and contain undeclared wheat. The recall was classified by the FDA on July 23, 2026, and added to the agency's Enforcement Report on July 24, 2026.
The products were distributed primarily to local restaurants in California, with some intended for retail in grocery stores via a wholesaler in New Mexico.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz
Reason: Undeclared colors: Yellow#5, and Yellow#6.
- UPC
- 757168 977315
Product details
Reason: No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.
Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16oz bags)/case. Wonton Wrappers packed into "Wonton Noodles Net Wt. 5 LBS" plastic bags and sold as 10 units (4-lb bags)/case. Neither product has ingredient labeling information.
Details
- Company began the recall
- Sold in
Firm distributes primarily to local restaurants (California) with some of the product intended for retail distribution in grocery stores via a wholesaler (New Mexico).
- Event ID
- 99386
- Recall numbers
- H-1187-2026 to H-1188-2026
- Company
- Man Fon, Inc.San Gabriel, California
- Recall type
- Voluntary: Firm initiated
- Customers told by
- Letter
Company began the recall
Classified by FDA
Added to FDA's Enforcement Report
Listed on Recall Canary
In FDA's weekly enforcement report
Recall ended
Summary updated
