Food/Recall·openFDA/food

Man Fon, Inc. — Class II: Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refriger

MediumPublished Jul 29, 2026· AI-analyzed Aug 3, 2026View original FDA source
AI-generated regulatory interpretation. The four sections below are an analyst-style summary produced by an AI model from the original FDA source. Always verify against the source before any regulatory, clinical, or commercial decision.
What happened

Man Fon, Inc. has initiated a Class II recall for its 'Won Ton Wrappers Extra Thin' (10 oz) due to undeclared color additives Yellow #5 and Yellow #6. The product was sold in cases of 48 units and requires refrigeration or freezing.

Who it affects

This affects Man Fon, Inc., food retailers carrying the specific UPC, and quality/regulatory personnel responsible for labeling accuracy in the refrigerated dough and pasta manufacturing sector.

Why it matters

A Class II recall indicates that the product may cause temporary or medically reversible adverse health consequences, or that the probability of serious adverse health consequences is remote. For regulatory professionals, this underscores the importance of stringent labeling controls regarding color additives, as failure to declare these substances constitutes a violation of FDA labeling requirements and necessitates formal market withdrawal.

Practical takeaway

QA teams should verify that all certified color additives, specifically Yellow #5 and Yellow #6, are explicitly declared on the ingredient statement. Immediate reconciliation of inventory for the affected UPC is required, and labeling audit protocols should be reviewed for compliance with allergen and additive disclosure requirements.

FDA source material

Class II. Reason: Undeclared colors: Yellow#5, and Yellow#6.. Product: Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refrigerated, Can be Frozen. Sold in 48 units (10oz)/case.. Firm: Man Fon, Inc. (San Gabriel CA United States). Status: Ongoing.

Open in openFDA / FDA.gov
AI-generated interpretation. Always verify critical decisions against the original FDA source. Generated with google/gemini-3-flash-preview.