CLASS II Food recall · Reported 26 Feb 2014 · FDA Enforcement Report

sauce for Char Sui recalled by Mid Pac Foods

Mid Pac Foods is recalling sauce for Char Sui, distributed in California, Hawaii, Nevada. The recall was initiated on 30 Jan 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots 10204 and 10247
Quantity recalled400 cases (12 units per case)

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-1539-2014
FDA event ID
67422
Recalling firm
Mid Pac Foods, Honolulu, HI
Classification
Class II
Status
Terminated
Recall initiated
30 Jan 2014
FDA classified
19 Feb 2014
Reported
26 Feb 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Sauces & Condiments

Timeline

30 Jan 2014Recall initiated by company
19 Feb 2014Classified by FDA+20 days
26 Feb 2014Published in enforcement report+7 days

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

Reason for recall

Inspection at firm found that sauce for Char Siu declares Hoisin sauce as an ingredient, but does not declare the sub ingredient of wheat.

Product as listed by the FDA

Mid Pac Foods brand sauce for Char Sui; Net 7 FL. oz (207 ml); Made in Hawaii, Keep in cool place UPC: 7336620250 Manufactured by Mid Pac Foods, Inc. Honolulu, HI.

Where it was distributed

HI,, CA. NV

CaliforniaHawaiiNevada

Questions about this recall

Why was it recalled?

Inspection at firm found that sauce for Char Siu declares Hoisin sauce as an ingredient, but does not declare the sub ingredient of wheat.

Which lots are affected?

Lots 10204 and 10247

Where was it sold?

HI,, CA. NV

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 26 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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