Food Recall Check
Class I · High risk Terminated Initiated Oct 11, 2012 (14 years ago)

Organic Toffee Peanuts recall

Recalled by Sconza Candy Company, Inc. · Oakdale, CA, United States

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

Why it was recalled

Sconza Candy Company is recalling organic toffee peanuts that were manufactured with peanuts from Sunland which are under recall because of the possibility of Salmonella contamination.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Organic Toffee Peanuts;Bulk packaging - 20 pound cases; Ingredients: Organic Peanuts, Organic Sugar, Salt.

Quantity: 35,660 pounds

Food: Nuts & seeds

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.

Item No, 600-72445 Lot No: 100401, 100402, 100514, 100624, 100907, 100908, 101112, 101115, 110413, 110614, 110718.

Where it was sold

Pennsylvania

FDA's distribution note: Product was only sold to one customer, Chris Candies, 1557 Spring Garden Avenue Pittsburg, PA 15212

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. 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
Sconza Candy Company, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 11, 2012
In FDA report of
Nov 21, 2012
Terminated
Mar 15, 2013
FDA recall number
F-0656-2013 · event 63452
Official record
FDA enforcement report search

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