Food Recall Check
Class I · High risk Terminated Initiated Apr 30, 2018 (8 years ago)

STONEWALL KITCHEN Basil Pesto Aioli recall

Recalled by Stonewall Kitchen, LLC · York, ME, United States

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

Why it was recalled

Product may contain undeclared eggs.

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

STONEWALL KITCHEN Basil Pesto Aioli Net Weight Net 10.25 oz. UPC: 7 11381 03060 8. Product is incorrectly labeled as Basil Pesto, Net Weight 8 oz.

Quantity: 732 units

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.

Enjoy By Date: 28SEP2019

Where it was sold

Alaska Arkansas Arizona California Colorado Connecticut Florida Illinois Massachusetts Minnesota Missouri North Carolina New Hampshire New Jersey New York Pennsylvania Texas Vermont Washington Wisconsin Wyoming

FDA's distribution note: AK, AR, AZ, CA, CO, CT, FL, IL, MA, MN, MO, NC, NH, NJ, NY, PA, TX, VT, WA, WI, WY

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
Stonewall Kitchen, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 30, 2018
In FDA report of
May 16, 2018
Terminated
Jun 26, 2018
FDA recall number
F-1440-2018 · event 79997
Official record
FDA enforcement report search

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