Food Recall Check
Class II · Moderate risk Terminated Initiated May 31, 2012 (14 years ago)

Broaster Fish Coating recall

Recalled by The Broaster Company, LLC · Beloit, WI, United States

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

Why it was recalled

The Broaster Company, LLC is recalling three lots of Broaster Fish Coating 96627 because they contain an undeclared color additive, Yellow Dye No. 6.

Undeclared allergen: Fish

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

Broaster Fish Coating, 96627, Ingredients: Corn Meal, Wheat Flour, Corn Crumbs, Salt, Spices, Paprika, Citric Acid, Onion, Sugar, Garlic, Celery Seed, Modified Con Starch, Lemon Oil, Natural and Artifical Flavors, Silicon Dioxide (Anti-Caking Agent) and FD&C yellow #5., Net Weight 20 pounds, Manufactured By The Broaster Company, Beloit, Wisconsin 53511.

Quantity: 89 (20 lbs cases)

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.

12-108-296 12-073-194 12-004-012

Where it was sold

Illinois Maryland Missouri Pennsylvania Wisconsin

FDA's distribution note: IL, MD, MO, WI, PA Egypt

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 fish; 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
The Broaster Company, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 31, 2012
In FDA report of
Jul 4, 2012
Terminated
Jul 2, 2012
FDA recall number
F-1655-2012 · event 61980
Official record
FDA enforcement report search

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