FDA recall record

Harry and David Operations 12 oz recall — FDA F-0561-2013

Product received from supplier is being recalled due to the potential to be contaminated with Salmonella

Class Iclassification
F-0561-2013official record ID
Nov 7, 2012report date

Recall record at a glance

Official recordF-0561-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHarry and David Operations, Inc.
Report dateNov 7, 2012
Recall initiation dateSep 27, 2012
Quantity5,928 - 12 oz. jars
LocationMedford, OR, United States

Official product description

Harry & David Creamy Caramel Peanut Spread, 12 oz. jars, labeled in part: "HARRY & DAVID CREAMY CARAMEL PEANUT SPREAD***NET WT 12 OZ (340g)***INGREDIENTS: ROASTEDPEANUTS, SUGAR, CARAMEL COMPOUND***MADE FOR: HARRY AND DAVID MEDFORD, OR 97501***7 80994 75786 8***" The 12 oz. jars are sold individually and also as gift add-ons for gift baskets. The gift baskets are listed below: Harry & David Apple Snack Box; Wolferman's Bee Sweet Gift Basket; Wolferman's Hearty Snack Gift Basket; Wolferman's All-Day Assortment Gift Basket; Wolferman's Fathers Day Basket

Why the product was recalled

Product received from supplier is being recalled due to the potential to be contaminated with Salmonella

Distribution information

Nationwide and Canada through online ordering www.harryanddavid.com/h/home and through retail stores located throught the U.S.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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