Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 5, 2014 (12 years ago)

Whalen's Seafood & Burger Sauce "hot" recall

Recalled by Whalen's Horseradish Products · Galway, NY, United States

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

Why it was recalled

Whalen's Seafood & Burger Sauce contains undeclared anchovies from the Worcestershire Sauce used in the finished product. The product also has miscellaneous labeling problems such as not all sub-ingredients are listed on finished product labeling.

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

WHALEN'S SEAFOOD & BURGER SAUCE "HOT", NET WT. 8 OZ. (226 g) -- Whalen's Horseradish Products, LLC, PO Box 4700, Saratoga Springs, New York 12866

Quantity: 36 bottles

Food: Sauces, dips & dressings

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.

Sell by Date of 17 July, 2015 (stamped on a label located on top of the bottle).

Where it was sold

Massachusetts New York

FDA's distribution note: NY and MA

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
Whalen's Horseradish Products
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 5, 2014
In FDA report of
Dec 24, 2014
Terminated
Feb 4, 2015
FDA recall number
F-0729-2015 · event 69966
Official record
FDA enforcement report search

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