CLASS I Food recall · Reported 25 Mar 2015 · FDA Enforcement Report

Go hyang Mak Kimchi recalled by Korean Food

Korean Food is recalling Go hyang Mak Kimchi (, distributed in Oklahoma, Texas. The recall was initiated on 23 Jan 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo lot code or manufacturing codes are applied to the products. Products manufactured 12/01/2014-01/23/2015.
Quantity recalled5 cases of 32 ounce; 5 cases of half gallon

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-1429-2015
FDA event ID
70353
Recalling firm
Korean Food, Irving, TX
Classification
Class I
Status
Terminated
Recall initiated
23 Jan 2015
FDA classified
17 Mar 2015
Reported
25 Mar 2015
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Product category
Other

Timeline

23 Jan 2015Recall initiated by company
17 Mar 2015Classified by FDA+53 days
25 Mar 2015Published 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

Product contains undeclared shellfish (shrimp)

Product as listed by the FDA

Go hyang Mak Kimchi 32 oz (UPC 042053138101) Product of U.S.A. TX. 972.790.4800 1311 Lukest, Irving, TX 75061; Go hyang Mak Kimchi 1/2 Gal (UPC 042053137302) Product of U.S.A. TX. 972.790.4800 1311 Lukest, Irving, TX. 75061

Where it was distributed

TX and OK

OklahomaTexas

Questions about this recall

Why was it recalled?

Product contains undeclared shellfish (shrimp)

Which lots are affected?

No lot code or manufacturing codes are applied to the products. Products manufactured 12/01/2014-01/23/2015.

Where was it sold?

TX and OK

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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