Class ITerminated in FDA datasetRecall initiated Jun 6, 2013

604293 Mega Omega Mix 12/8 Oz Sq Tub

Recalling firm: Bergin Fruit And Nut Co Inc

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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 15, 2014.

Check your package

Compare the exact product and package details with the label you have.

Product604293 MEGA OMEGA MIX 12/8 OZ SQ TUB, UPC 2052604293 604293.04 MEGA OMEGA MIX 12/8 OZ SQ TUB BOULDER, UPC 2052604293 604293.05 MEGA OMEGA MIX 12/8 OZ SQ TUB FESTIVAL, UPC 2052604293 604290 MEGA OMEGA MIX 15#, UPC 2052604290 604292 MEGA OMEGA MIX 16/7 OZ - CLAMSHELL,UPC 2052604292 604291 MEGA OMEGA MIX 5#, UPC 2052604291
Package size8 OZ

FDA code information

11/26/13, 1/11/2014, 1/19/2014,1/11/2014, 1/22/2014, 1/28/2014, 1/29/2014.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

604293 MEGA OMEGA MIX 12/8 OZ SQ TUB, UPC 2052604293 604293.04 MEGA OMEGA MIX 12/8 OZ SQ TUB BOULDER, UPC 2052604293 604293.05 MEGA OMEGA MIX 12/8 OZ SQ TUB FESTIVAL, UPC 2052604293 604290 MEGA OMEGA MIX 15#, UPC 2052604290 604292 MEGA OMEGA MIX 16/7 OZ - CLAMSHELL,UPC 2052604292 604291 MEGA OMEGA MIX 5#, UPC 2052604291

Original FDA recall reason

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.

Recall details

Recall number
F-1738-2013
Event ID
65545
FDA status
Terminated
Initiated
Jun 6, 2013
Reported
Jul 31, 2013
Classified
Jul 23, 2013
Terminated
Jan 15, 2014
Quantity
331.3
Location
Saint Paul, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

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

FDA source record · F-1738-2013

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.