Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 22, 2016 (10 years ago)

Ambrosia Quality Foods recall

Recalled by Schreiber Food International · Upper Saddle River, NJ, United States

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

Why it was recalled

Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.

Undeclared allergen: Peanut

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

Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz.

Quantity: 5828 jugs

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.

1512163592 12/15/2016 1603289943 3/28/2017 1604292400 4/29/2017 1605244146 5/24/2017 1607259420 7/25/2017 1608020141 8/2/2017 1608100780 8/10/2017 1607077741 7/7/2017 1608020141 8/2/2017 1608040416 8/4/2017 1608100780 8/10/2017 1608100780 8/10/2017 1608262208 8/26/2017 1609275267 9/27/2017 1610268040 10/26/2017

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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 peanut; 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
Schreiber Food International
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 22, 2016
In FDA report of
Feb 1, 2017
Terminated
Apr 13, 2017
FDA recall number
F-1339-2017 · event 76155
Official record
FDA enforcement report search

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