CLASS II Food recall · Reported 13 Dec 2017 · FDA Enforcement Report

Woldong World's Best Kimchi Whole Cabbage Kimchi Premium recalled

H. A. R. Maspeth is recalling Woldong World's Best Kimchi Whole Cabbage Kimchi Premium, distributed in 9 states. The recall was initiated on 27 Nov 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes8633-24, 8633-25, 8633-26, 8633-27, 8633-28, 8633-29
Quantity recalled3lb: 150 pieces and 7lb: 170 pieces

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-0430-2018
FDA event ID
78639
Recalling firm
H. A. R. Maspeth, Maspeth, NY
Classification
Class II
Status
Terminated
Recall initiated
27 Nov 2017
FDA classified
6 Dec 2017
Reported
13 Dec 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sesame
Product category
Other

Timeline

27 Nov 2017Recall initiated by company
6 Dec 2017Classified by FDA+9 days
13 Dec 2017Published 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

Product contains undeclared sesame seeds.

Product as listed by the FDA

WOLDONG WORLD'S BEST KIMCHI WHOLE CABBAGE KIMCHI PREMIUM 3LBS (1.36kg), UPC: 8 46034 04853 9 and 7LBS (3.17kg), UPC: 846034048546.

Where it was distributed

NY, NJ, VA, MD, MA, PA, GA, IL, TX

GeorgiaIllinoisMassachusettsMarylandNew JerseyNew YorkPennsylvaniaTexasVirginia

Questions about this recall

Why was it recalled?

Product contains undeclared sesame seeds.

Which lots are affected?

8633-24, 8633-25, 8633-26, 8633-27, 8633-28, 8633-29

Where was it sold?

NY, NJ, VA, MD, MA, PA, GA, IL, 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 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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