601009 ANTIOXIDANT SUPERSTAR MIX 100/2 OZ FLAT PACK
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 manufacturing using pistachios supplied by ARO Pistachio Company. The recall was initiated because Salmonella was found in the environment at the ARO Pistachio Company.
The exact product
601009 ANTIOXIDANT SUPERSTAR MIX 100/2 OZ FLAT PACK, UPC 2052601009 601076 ANTIOXIDANT SUPERSTAR MIX 12/6 OZ BERGIN RED BAG, UPC 2052601076 601051 ANTIOXIDANT SUPERSTAR MIX 12/8 OZ CLAMSHELL, UPC 2052601051 601051.03 ANTIOXIDANT SUPERSTAR MIX 12/8 OZ CLAMSHELL KOWALSKI, UPC 2052601051 601049.01 ANTIOXIDANT SUPERSTAR MIX 16/6 OZ CLAMSHELL, UPC 1115099870 601049.1 ANTIOXIDANT SUPERSTAR MIX 16/6 OZ CLAMSHELL CUB, IUPAC 601070 ANTIOXIDANT SUPERSTAR MIX 3/5#, UPC 2052601070 601050 ANTIOXIDANT SUPERSTAR MIX 30#, UPC 2052601050 601052 ANTIOXIDANT SUPERSTAR MIX 5#, UPC 2052601052 601069 ANTIOXIDANT SUPERSTAR MIX 8/10 OZ SQ TUB, UPC 2052601069 601069.05 ANTIOXIDANT SUPERSTAR MIX 8/10 OZ SQ TUB FESTIVAL, UPC 2052601069 601054 ANTIOXIDANT SUPERSTAR MX 12/10 OZ BAGLINE, UPC 2052601054 601069.04 ANTIOXIDANT SUPERSTAR MIX 8/10 OZ SQ TUB BOULDER, IUPAC 601048.00 ANTIOXIDANT SUPERSTAR MIX 100/2 OZ FLAT PACK PROMOTIONAL ANTIOXIDANT SUPERSTAR MIX***, UPC 2052601048. 601049.00 ANTIOXIDANT SUPERSTAR MIX 16/6 OZ CLAMSHELL SUPER ANTIOXIDANT MIX***, UPC 2052601049 612150.03 LARGE GIFT BOX KOWALSKIS, UPC 2052612150.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Best By 6/22/2013, 10/6/2013, 10/10/2013,10/30/2013, 12/29/2013, 1/8/2014, 1/12/2014, 2/1/14, 2/2/2014, 1/26/2014, 1/28/2014.
| Type | Code / value | Context |
|---|---|---|
| best by | 6/22/2013 | Best By 6/22/2013, 10/6/2013, 10/10/2013,10/30/2013, 12/29/2013, 1/8/2014, 1/12/2014, 2/1/14, 2/2/2014, 1/26/2014, 1/28/2014. |
Recall details
- Recall number
- F-1734-2013
- Event ID
- 65545
- FDA status
- Terminated
- Initiated
- Jun 6, 2013
- Reported
- Jul 31, 2013
- Classified
- Jul 23, 2013
- Terminated
- Jan 15, 2014
- Quantity
- 1705.55
- 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.
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.