Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 5, 2016 (11 years ago)

Land O Lakes recall

Recalled by Ventura Foods LLC · Saint Joseph, MO, United States

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

Why it was recalled

Cases of 5 gram portion cups of margarine for the food service market were distributed without label information. The cups therefore failed to disclose the margarine contained the allergens milk and soy.

Undeclared allergens: Milk Soy

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

Land O Lakes, Fresh Buttery Taste Spread, 48% Vegetable Oil Spread, A product of Land O'Lakes Inc. Arden Hills, MN. Packaged in 5 gram plastic cups.

Quantity: 96/920/5 grams/individual cups/cases

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.

Production date J28115 Lot number 150528116

Where it was sold

Kentucky Louisiana Tennessee

FDA's distribution note: One distribution center in Tennessee. Product was further distributed to other distribution centers in Tennessee, Kentucky, and Louisiana.

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 milk, soy; 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
Ventura Foods LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 5, 2016
In FDA report of
Mar 16, 2016
Terminated
Apr 26, 2016
FDA recall number
F-0723-2016 · event 73250
Official record
FDA enforcement report search

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