Recall record at a glance
| Official record | F-1742-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bergin Fruit And Nut Co Inc. |
| Report date | Jul 31, 2013 |
| Recall initiation date | Jun 6, 2013 |
| Quantity | 914.05 |
| Location | Saint Paul, MN, United States |
Official product description
603684 PISTACHIOS S/I/S 12/10 OZ GOLD BAG, UPC 2052603684 600913 PISTACHIOS S/I/S 12/12 OZ BAGLINE, UPC 2052600913 600913.11 PISTACHIOS S/I/S 12/12 OZ BAGLINE AMAZON, UPC 2052600913 600913.07 PISTACHIOS S/I/S 12/12 OZ BAGLINE DISPLAY BOX, UPC 2052600913 600923.05 PISTACHIOS S/I/S 12/12 OZ BAGLINE FESTIVAL, UPC 2052600923 600915 PISTACHIOS S/I/S 12/12 OZ TRAY, UPC 2052600915 603672 PISTACHIOS S/I/S 12/26 OZ TIN HOLIDAY CLOSED SLEEVE, UPC 2052603672 600921 PISTACHIOS S/I/S 12/8 OZ CLAMSHELL, UPC2052600921 603667 PISTACHIOS S/I/S 16/15 OZ TIN HOLIDAY CLOSED SLEEVE, UPC 2052603667 600912 PISTACHIOS S/I/S 25#, UPC 2052600912 600914 PISTACHIOS S/I/S 4/20 OZ TUB, UPC 2052600914 600914.03 PISTACHIOS S/I/S 4/20 OZ TUB KOWALSKI, UPC 2052600914 603677 PISTACHIOS S/I/S 4/36 OZ TIN HOLIDAY CLOSED SLEEVE, UPC 2052603677 603902 PISTACHIOS S/I/S 4/36 OZ TIN HOLIDAY OPEN SLEEVE, UPC2052603902 600911 PISTACHIOS S/I/S 5#, UPC 2052600911 600927.04 PISTACHIOS S/I/S 8/8 OZ SQ TUB BOULDER, UPC 2052600927 600927.05 PISTACHIOS S/I/S 8/8 OZ SQ TUB FESTIVAL, UPC 2052600927 601912 PISTACHIOS S/IS 10/14 OZ TAPE BAG, UPC2052601912 601912.09 PISTACHIOS S/IS 10/14 OZ TAPE BAG BYERLYS, UPC 2052601912 601912.08 PISTACHIOS S/IS 10/14 OZ TAPE BAG LUNDS, UPC 2052601912 603858.00 PISTACHIOS S/I/S 12/26 OZ OPEN SLEEVE IN SHELL PISTACHIOS, UPC 2052603858.
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
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