RecallHawk
Class II Recall

Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16oz bags)/case. Wonton Wrappers packed in

Man Fon, Inc.

Summary

The FDA issued a Class II for Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16o by Man Fon, Inc.. Reason: No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6..

Details

Source

Food Recall

External ID

H-1188-2026

Action Date

2026-07-29

Status

Ongoing

Category

food

Product Description

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.

Lot/Code Info: No lot codes.

Quantity Affected: 40 lbs (4-lb size only)

Reason for Recall

No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.

Distribution

Firm distributes primarily to local restaurants (CA) with some of the product intended for retail distribution in grocery stores via a wholesaler (NM).

Type: Voluntary: Firm initiated

Recall Initiated: 2026-07-08

Company

Man Fon, Inc.

San Gabriel, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 37 food recalls issued in the same week, part of 60 food-related FDA actions this month.

Man Fon, Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Man Fon, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Man Fon, Inc. have FDA actions?

Man Fon, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1188-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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