Giai Phat Shrimp Ball recall

Recalled by Chaur Fong Inc. dba 888 Food Company · South El Monte, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared egg

Undeclared allergen: Egg

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Giai Phat Shrimp Ball NET Wt. 7 oz. (198g) Keep Frozen Open Packaging Before Thawing Item #30108 Ingredients: Shrimp (surimi), Water, Tapioca Flour, Salt, Sugar, Monosodium, Glutamate, Garlic Powder, White Pepper, Baking Powder, Spice, Sesame Oil, and Red #40 Food Color Manufactured By: 888 Food Co. S. EL Monte, CA 91733

Quantity: 335,401 bags (total)

Food: Seafood & fish

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Numbers: 551521, 551731, 552081, 552221, 552571, 552781, 553201, 553481, 550042, 550182, 550462, 550742, 550952, 551092, 551442

Where it was sold

California Idaho Illinois

FDA's distribution note: U.S. distribution to the following: CA, IL, and ID No foreign distribution.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Chaur Fong Inc. dba 888 Food Company
Initiated by: Voluntary: Firm initiated
Recall initiated: Jun 9, 2022
In FDA report of: Jun 29, 2022
Terminated: Jan 31, 2023
FDA recall number: F-1355-2022 · event 90425
Official record: FDA enforcement report search