CLASS I Food recall · Reported 2 Aug 2017 · FDA Enforcement Report

Lam Sheng Kee Frozen Fried Fish Ball recalled by Global Lam Sheng Kee

Global Lam Sheng Kee is recalling Lam Sheng Kee Frozen Fried Fish Ball, distributed in 12 states. The recall was initiated on 20 Apr 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lots that do not declare egg.
Quantity recalledExact quantity is unknown.

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-2814-2017
FDA event ID
77583
Recalling firm
Global Lam Sheng Kee, Brooklyn, NY
Classification
Class I
Status
Terminated
Recall initiated
20 Apr 2017
FDA classified
21 Jul 2017
Reported
2 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Egg
Product category
Fish

Timeline

20 Apr 2017Recall initiated by company
21 Jul 2017Classified by FDA+92 days
2 Aug 2017Published in enforcement report+12 days

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

Reason for recall

Product may contain undeclared egg.

Product as listed by the FDA

Lam Sheng Kee Frozen Fried Fish Ball NET WEIGHT: 227g (8oz)

Where it was distributed

MI, PA, NC, VA, TX, IL, NY, NJ, FL, OH, CA, CO

CaliforniaColoradoFloridaIllinoisMichiganNorth CarolinaNew JerseyNew YorkOhioPennsylvaniaTexasVirginia

Questions about this recall

Why was it recalled?

Product may contain undeclared egg.

Which lots are affected?

All lots that do not declare egg.

Where was it sold?

MI, PA, NC, VA, TX, IL, NY, NJ, FL, OH, CA, CO

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.

Other products in this recall event

2 other products · FDA event 77583

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