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FDA source record Class I Terminated

Giai Phat Featherback Fish Ball NET WT. 11 oz. (312g) Ingredients: Fish meat (may contain Surimi (Japanese Threadfin Bream, Sugar, Polyphosphate) Lady Fish and or Featherback F...

Recall Date: 2022-06-09 Recalling Firm: Chaur Fong Inc. dba 888 Food Company Record Ref: F-1352-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Giai Phat Featherback Fish Ball NET WT. 11 oz. (312g) Ingredients: Fish meat (may contain Surimi (Japanese Threadfin Bream, Sugar, Polyphosphate) Lady Fish and or Featherback F... and names Chaur Fong Inc. dba 888 Food Company as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Chaur Fong Inc. dba 888 Food Company
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2022-06-09
Best identifiers to check for a FDA record

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Product Description & Identification

Giai Phat Featherback Fish Ball NET WT. 11 oz. (312g) Ingredients: Fish meat (may contain Surimi (Japanese Threadfin Bream, Sugar, Polyphosphate) Lady Fish and or Featherback Fish) Water, Tapioca Flour, Salt, Monosodium Glutamate, Garlic Powder, White Pepper, Baking Powder (Sodium Acid, Bicarbonate, Corn Starch, and Monocalcium Phosphate), and Spice. Keep Product Refrigerated at 38F or Below. May Be Frozen Item # 21113 Distributed By: 888 Food CO. S. El Monte, CA 91733

Reason for Recall / Hazard Identified

Undeclared egg

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

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Consumer Action Recorded in the Source

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Distribution & Affected States

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

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1352-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
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