CLASS I Food recall · Reported 28 Nov 2012 · FDA Enforcement Report

Spinach Feta Dip recalled by Sartori Inspirations

Sartori Inspirations is recalling Spinach Feta Dip, distributed nationwide in the US. The recall was initiated on 20 Jul 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot number FS21931.
Quantity recalled5 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-0719-2013
FDA event ID
62629
Recalling firm
Sartori Inspirations, Lafayette, CO
Classification
Class I
Status
Terminated
Recall initiated
20 Jul 2012
FDA classified
21 Nov 2012
Reported
28 Nov 2012
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Listeria
Product category
Dips & Spreads

Timeline

20 Jul 2012Recall initiated by company
21 Nov 2012Classified by FDA+124 days
28 Nov 2012Published in enforcement report+7 days

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

Reason for recall

Sartori is recalling various dips, salsas, and cheese products which may have been manufactured onion mixes which were recalled by another firm due to possible contamination with Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Spinach Feta Dip packaged in 7 oz clear plastic containers, manufactured by Sartori Inspirations, LLC, Lafayette, CO 80026.

Where it was distributed

Distributed to Whole Foods Grocery chain only with nationwide locations including Rocky Mountain, Northeast, North Atlantic, Mid Atlantic, Northwest, and Southwest.

Nationwide

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Sartori is recalling various dips, salsas, and cheese products which may have been manufactured onion mixes which were recalled by another firm due to possible contamination with Listeria monocytogenes.

Which lots are affected?

Lot number FS21931.

Where was it sold?

Distributed to Whole Foods Grocery chain only with nationwide locations including Rocky Mountain, Northeast, North Atlantic, Mid Atlantic, Northwest, and Southwest.

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

Other products in this recall event

9 other products · FDA event 62629

This product is part of a recall event; the main page for the event is Smoked Gouda recalled by Sartori Inspirations.

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