Food Recall Check
Class I · High risk Terminated Initiated Jul 30, 2012 (14 years ago)

Trader Giotto brand Pesto Pizza in recall

Recalled by Amy'S Kitchen · Petaluma, CA, United States

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

Why it was recalled

Product contains undeclared peanut in the ingredient statement (Peanuts were found in pinenuts).

Undeclared allergen: Peanut

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

Trader Giotto brand Pesto Pizza in 13.5 oz; SKU# 00539937; Product is processed and packaged by Amy's Kitchen, White City, Oregon

Quantity: N/A

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.

Best Before July 17, 2012 and July 18, 2012; Lot Code: 30-1992AK and 30-2002AK

Where it was sold

California Illinois Pennsylvania Tennessee

FDA's distribution note: Products were released for distribution in US (PA, TN, IL, CA).

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 peanut; 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
Amy'S Kitchen
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 30, 2012
In FDA report of
Sep 5, 2012
Terminated
Oct 31, 2012
FDA recall number
F-2080-2012 · event 62759
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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