Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 22, 2019 (7 years ago)

QQ Fish brand SHRIMP FLAVOURED SEAFOOD BALL recall

Recalled by Great One Trading Inc. · Brooklyn, NY, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product contains an undeclared allergen, specifically egg, that is not listed in the ingredient statement.

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

QQ Fish brand SHRIMP FLAVOURED SEAFOOD BALL; Net weight 200g/7oz

Quantity: Shrimp Flavored: 40 cartons; 50-200g packets/carton; total: 2,000 packets

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.

UPC Code: 8886323239028; Exp: 01/19/2020

Where it was sold

Connecticut Massachusetts Pennsylvania

FDA's distribution note: Products were distributed in: MA, PA, CT

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Great One Trading Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 22, 2019
In FDA report of
Sep 18, 2019
Terminated
Aug 4, 2020
FDA recall number
F-0006-2020 · event 83624
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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