CLASS II Food recall · Reported 13 Feb 2013 · FDA Enforcement Report

Yangchun Noodles, 12 bgs recalled by Man Fon

Man Fon is recalling Yangchun Noodles, 12 bgs, distributed in Texas. The recall was initiated on 8 Jan 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesno lot number available
Quantity recalled120 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0979-2013
FDA event ID
35908
Recalling firm
Man Fon, San Gabriel, CA
Classification
Class II
Status
Terminated
Recall initiated
8 Jan 2013
FDA classified
5 Feb 2013
Reported
13 Feb 2013
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Product category
Pasta & Noodles

Timeline

8 Jan 2013Recall initiated by company
5 Feb 2013Classified by FDA+28 days
13 Feb 2013Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Man Fon is recalling Yangchun Noodles because they contain undeclared wheat allergen.

Product as listed by the FDA

Yangchun Noodles, 10 case, 12 bgs per case

Where it was distributed

TX

Texas

Questions about this recall

Is Yangchun Noodles, 12 bgs recalled?

Yes. Man Fon recalled Yangchun Noodles, 12 bgs on 8 Jan 2013. The recall is Class II and its status is Terminated. Recall number F-0979-2013.

Why was it recalled?

Man Fon is recalling Yangchun Noodles because they contain undeclared wheat allergen.

Which lots are affected?

no lot number available

Where was it sold?

TX

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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