FDA recall record

Bergin Fruit And Nut Co 601041 HEALTHY HEART MIX 12/14 OZ TRAY, UPC 2052601041 601078 recall — FDA F-1735-2013

Bergin Fruit and Nut Company is initiating a recall on a number of pistachio products manufactured using pistachios supplied by ARO Pistachio Inc.…

Class Iclassification
F-1735-2013official record ID
Jul 31, 2013report date

Recall record at a glance

Official recordF-1735-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmBergin Fruit And Nut Co Inc.
Report dateJul 31, 2013
Recall initiation dateJun 6, 2013
Quantity1527.59
LocationSaint Paul, MN, United States

Official product description

601041 HEALTHY HEART MIX 12/14 OZ TRAY, UPC 2052601041 601078 HEALTHY HEART MIX 12/8 OZ CLAMSHELL, UPC 2052601078 601078.03 HEALTHY HEART MIX 12/8 OZ CLAMSHELL KOWALSKI, UPC 2052601078 601089 HEALTHY HEART MIX 16/6 OZ CLAMSHELL, UPC 2052601089 601089.1 HEALTHY HEART MIX 16/6 OZ CLAMSHELL CUB, UPC 1115099868 601125 HEALTHY HEART MIX 8/10 OZ SQ TUB, UPC 2052601125 601125.04 HEALTHY HEART MIX 8/10 OZ SQ TUB BOULDER, UPC 2052601125 601125.05 HEALTHY HEART MIX 8/10 OZ SQ TUB FESTIVAL, UPC 2052601125 601063 HEALTHY HEART NUT MIX 12/16 OZ BAGLINE, UPC 2052601063 601061.05 HEALTHY HEART NUT MIX 12/16 OZ FESTIVAL, UPC 2052601061 601037 HEALTHY HEART NUT MIX 30#, UPC 2052601037 601038 HEALTHY HEART NUT MIX 5#, UPC 2052601038 601089.01 HEALTHY HEART MIX 16/6 OZ CLAMSHELL, UPC 1115099868 602037 HEALTHY HEART NUT MIX 2/5#, UPC 2052602037 601137.00 HEALTHY HEART MIX 12/7 OZ BERGIN CUSTOM ZIPLOCK POUCH DISCONTINUED HEALTHY HEART MIX***, UPC 2052601137

Why the product was recalled

Bergin Fruit and Nut Company is initiating a recall on a number of pistachio products manufactured using pistachios supplied by ARO Pistachio Inc. Salmonella was found in the environment at the ARO Pistachio Inc. company.

Distribution information

CA, ID, IL, IN, IA, KS, KY, MI, MN, NV, ND, PA, SD, TN, WI.

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: Letter.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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