Food Recall Check
Class I · High risk Terminated Initiated Oct 4, 2012 (14 years ago)

Ma Baensch Marinated Herring in Wine Sauce recall

Recalled by Wild Foods, Inc · Milwaukee, WI, United States

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

Why it was recalled

Labeling error. One date code of 24 oz. Baensch Marinated Herring in Wine Sauce may contain an undeclared milk allergen.

Undeclared allergen: Milk

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

Ma Baensch Marinated Herring in Wine Sauce, Net Wt. 24 oz.. (680g), UPC 714449-10220 in glass jars with gold metal lids.

Quantity: 144 jars

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 and Lot Code: BEST IF USED BY 06NOV12 158. (printed in black ink on the top of the gold lid)

Where it was sold

Illinois Wisconsin

FDA's distribution note: retail stores in WI and Rockford, IL

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 milk; 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
Wild Foods, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 4, 2012
In FDA report of
Nov 7, 2012
Terminated
Jun 2, 2017
FDA recall number
F-0558-2013 · event 63409
Official record
FDA enforcement report search

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