Recall record at a glance
| Official record | F-2269-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Aurora Products, Inc. |
| Report date | May 20, 2015 |
| Recall initiation date | Mar 20, 2015 |
| Quantity | 8362.4 |
| Location | Orange, CT, United States |
Official product description
Roasted Salt Mixed Nuts: Aurora, 4.5 oz. Plastic Pouch, UPC: 65585200252; Aurora, 20 oz. Plastic Tub, UPC: 65585200340; Aurora, 10 oz. Plastic Pouch, UPC: 65585200804, Aurora, Bulk, No UPC, Belmont Market, 20 oz. Plastic Tub, UPC: 65585200340, Food Emporium Brand Products, 6.5 oz. Gift Bag, UPC: 1119079042; Food Emporium Brand Products, 20 oz. Plastic Tub, UPC: 1119079095, Gauls Market Brand Products, 20 oz. Plastic Tub, UPC: 65585200340; Giant Carlisle Food Store, 9.0 oz. Plastic Cup, UPC: 68826714736; Giant of Maryland, 9.0 oz. Plastic Cup, UPC: 68826714736; Martins Food, 9.0 oz. Plastic Cup, UPC: 68826714736; Stop&Shop, 9.0 oz. Plastic Cup, UPC: 68826714736; Aurora, 9.0 oz. Plastic Cup, UPC: 65585200084; Ernest Klein, 9.0 oz. Plastic Cup, UPC: 65585200084; Gauls Market Brand Products, 9.0 oz. Plastic Cup, UPC: 65585200084; Harvest Co Op Market, 9.0 oz. Plastic Cup, UPC: 65585200084; Hurley Ridge, 9.0 oz. Plastic Cup, UPC: 65585200084 11/4/15 12/13/15 Palmers Market Roasted Salt Mixed Nuts 9.0 oz. Plastic Cup 65585200084 11/4/15 12/13/15 Wild Acorns Roasted Salt Mixed Nuts 9.0 oz. Plastic Cup 81957401052 11/4/15 12/13/15 Wild By Nature Brand Products Roasted Salt Mixed Nuts 9.0 oz. Plastic Cup 65585270084 11/4/15 12/10/15; Gourmet Garage, 9 oz. Plastic Cup, UPC: 79084505922; Gourment Garage, 20 oz. Plastic Tub, UPC: 79084505842
Why the product was recalled
Salmonella
Distribution information
Product shipped to distributors in the following states: NY, CT, NH, RI, MA, CA, MD, ME, MN, PA and Nationwide through retail stores. Canada: Winners, HomeSense and Marshalls stores Bermuda
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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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