CLASS I Food recall · Reported 25 Oct 2017 · FDA Enforcement Report

Spinach Artichoke & Parmesan Dip & Spread recalled by La Terra Fina

La Terra Fina is recalling La Terra Fina Spinach Artichoke & Parmesan Dip & Spread, distributed in 12 states. The recall was initiated on 10 Oct 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot number: 20170912 Use By Date: NOV-01-2017
Quantity recalled2125 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0024-2018
FDA event ID
78247
Recalling firm
La Terra Fina, Union City, CA
Classification
Class I
Status
Terminated
Recall initiated
10 Oct 2017
FDA classified
17 Oct 2017
Reported
25 Oct 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Dips & Spreads

Timeline

10 Oct 2017Recall initiated by company
17 Oct 2017Classified by FDA+7 days
25 Oct 2017Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared allergen; egg.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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

Where it was distributed

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

CaliforniaColoradoFloridaGeorgiaIndianaMassachusettsMarylandNew JerseyNew YorkPennsylvaniaTexasWisconsin

Questions about this recall

Is Spinach Artichoke & Parmesan Dip & Spread recalled?

Yes. La Terra Fina recalled Spinach Artichoke & Parmesan Dip & Spread on 10 Oct 2017. The recall is Class I and its status is Terminated. Recall number F-0024-2018.

Why was it recalled?

Undeclared allergen; egg.

Which lots are affected?

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

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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