Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 14, 2013 (14 years ago)

Bulk Creamy/Smooth Peanut butter recall

Recalled by Producers Peanut Company Inc · Suffolk, VA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Peanut butter may contain aflatoxins above allowable levels.

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

Bulk Creamy/Smooth Peanut butter, packed in plastic 4 lb tub, packed 6 tubs/box; 5 lb tub, packed 6 tubs/box, and 35 lb buckets under private labels: Peanut Kids, Eden and American Farm Peanut Butters, and labeled in part ***Manufactured by Producers Peanut Co., Inc. 337 Moore Ave., Suffolk, VA 23434***

Quantity: 1101- 4 lb tubs; 573- 5 lb tubs; 181- 35 lb buckets; Total 49,949 lb

Food: Peanut butter

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.

2/12/2013, 2/13/2013, POD FEB 12 2013, POD FEB 2013, and 01.13.2015

Where it was sold

Illinois Maryland New York Virginia

FDA's distribution note: Distributed in New York, Virginia, Illinois, Maryland, and exported to Barbados.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Producers Peanut Company Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 14, 2013
In FDA report of
Apr 10, 2013
Terminated
Jun 21, 2013
FDA recall number
F-1293-2013 · event 64717
Official record
FDA enforcement report search

Also recalled with it (3 more products)

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

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