Class IF-1735-2013

Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.

Product

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

Type: Food
Affected lot / code info: Best By: 11/20/2013, 12/11/2013, 11/23/2013, 1/28/2014, 1/11/2014, 1/12/2014, 1/18/2014, 1/21/2014, 1/22/2014, 1/29/2014, 2/2/2014.
Quantity: 1527.59

Why it 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.

Recalling firm

Firm: Bergin Fruit And Nut Co Inc
Notification channel: Letter
Type: Voluntary: Firm initiated
Address: 2000 Energy Park Dr, N/A, Saint Paul, Minnesota 55108-1506

Distribution

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

Timeline

Recall initiated: 2013-06-06
FDA classified: 2013-07-23
Posted by FDA: 2013-07-31
Terminated: 2014-01-15
Status: Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-1735-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings.