Food Recall Check
Class I · High risk Terminated Initiated Oct 10, 2017 (9 years ago)

La Terra Fina Spinach Artichoke & Parmesan Dip & Spread recall

Recalled by La Terra Fina, Inc. · Union City, CA, United States

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

Why it was recalled

Undeclared allergen; egg.

Undeclared allergen: Egg

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

La Terra Fina Spinach Artichoke & Parmesan Dip & Spread NET WT. 10 oz. (.625 lb.) 284g UPC 6-40410-51327-3

Quantity: 2125 cases

Food: Cheese Leafy greens & salads 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.

Lot number: 20170912 Use By Date: NOV-01-2017

Where it was sold

California Colorado Florida Georgia Indiana Massachusetts Maryland New Jersey New York Pennsylvania Texas Wisconsin

FDA's distribution note: U.S. distribution to the following: CA, NJ, CO, GA, FL, MD, PA, MA, IN, WI, TX, and NY. No foreign distribution.

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 egg; 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
La Terra Fina, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 10, 2017
In FDA report of
Oct 25, 2017
Terminated
Dec 5, 2017
FDA recall number
F-0024-2018 · event 78247
Official record
FDA enforcement report search

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