Food Recall Check
Class I · High risk Terminated Initiated Nov 13, 2018 (8 years ago)

Purveyors Kitchen Pumpkin Pesto Tapenade recall

Recalled by Nor Cal Food Solutions LLC · Auburn, CA, United States

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

Why it was recalled

Pumpkin Pesto does not declare walnuts as ingredient or allergen.

Undeclared allergen: Tree nuts

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

Purveyors Kitchen Pumpkin Pesto Tapenade; NET WT 7.75 oz. (220G) UPC: 0 37677 01624 9 Ingredients: Water, Pumpkin, Basil, Parsley, Canola Oil, Sugar, Garlic, Parmesan Cheese (pasteurized skim milk, cultures, salt, enzymes), Lemon juice [concentrate], Sea Salt, Spices. Manufactured by: Purveyors Kitchen, Auburn, CA

Quantity: 567 cases

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.

PKPP17179A PKPP17179B PKPP17179C PKPP17230B Expiration dates: June 2019 and August 2019

Where it was sold

California Virginia

FDA's distribution note: CA and VA

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 tree nuts; 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
Nor Cal Food Solutions LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 13, 2018
In FDA report of
Dec 5, 2018
Terminated
Mar 1, 2019
FDA recall number
F-0679-2019 · event 81567
Official record
FDA enforcement report search

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