CLASS I Food recall · Reported 29 Jun 2022 · FDA Enforcement Report

Giai Phat Cuttle Fish Ball recalled by Chaur Fong

Chaur Fong is recalling Giai Phat Cuttle Fish Ball, distributed in California, Illinois. The recall was initiated on 9 Jun 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot Numbers: 561591, 561941, 562291, 562361, 562641, 562851, 563271, 560532, 560812, 561022, 561302
Quantity recalled335,401 bags (total)

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-1354-2022
FDA event ID
90425
Recalling firm
Chaur Fong, South El Monte, CA
Classification
Class I
Status
Terminated
Recall initiated
9 Jun 2022
FDA classified
23 Jun 2022
Reported
29 Jun 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Egg
Product category
Flour

Timeline

9 Jun 2022Recall initiated by company
23 Jun 2022Classified by FDA+14 days
29 Jun 2022Published in enforcement report+6 days

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

Reason for recall

Undeclared egg

Product as listed by the FDA

Giai Phat Cuttle Fish Ball NET WT. 8 oz. (227g) Keep Frozen Open Package Before Thawing Item # 31108 Ingredients: Cuttle Fish, Surimi (Japanese Threadfin Bream Fish, Sugar, Polyphosphate), Water, Tapioca Flour, Salt, Monosodium Glutamate, Garlic Powder, White Pepper, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and Monocalcium Phosphate) and Spice Distributed By: 888 Food Co. S. El Monte, CA 91733

Where it was distributed

U.S. distribution to the following: CA, IL, and ID No foreign distribution.

CaliforniaIllinois

Questions about this recall

Why was it recalled?

Undeclared egg

Which lots are affected?

Lot Numbers: 561591, 561941, 562291, 562361, 562641, 562851, 563271, 560532, 560812, 561022, 561302

Where was it sold?

U.S. distribution to the following: CA, IL, and ID No foreign distribution.

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

6 other products · FDA event 90425

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