Roasted Salt Mixed Nuts: Aurora, 4.5 oz
Food recall F-2269-2015. Published in FDA’s Enforcement Report on May 20, 2015.
- FDA Class I
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on May 20, 2015. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 10 states named
- 8362.4 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class I, the most serious of FDA’s three classes.
“Dangerous or defective products that predictably could cause serious health problems or death. Examples include: food found to contain botulinum toxin, food with undeclared allergens, a label mix-up on a lifesaving drug, or a defective artificial heart valve.”
openFDA, in plain words, its enforcement report fields.
“Class I is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
FDA’s rule, 21 CFR 7.3(m)(1), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Salmonella
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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
8362.4, in FDA’s words.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Best if used by date range: 11/18/15 12/19/15
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Barcodes and drug codes
-
UPC
65585200252 -
UPC
65585200340 -
UPC
65585200804 -
UPC
1119079042 -
UPC
1119079095 -
UPC
68826714736 -
UPC
65585200084 -
UPC
6558520008411 -
UPC
79084505922 -
UPC
79084505842
As FDA’s description and codes give them; the UPCs written as digits only.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
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
The states and territories these words name
- California
- Connecticut
- Massachusetts
- Maryland
- Maine
- Minnesota
- New Hampshire
- New York
- Pennsylvania
- Rhode Island
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Mar 20, 2015.
- FDA classified it on May 12, 2015.
- FDA’s Enforcement Report published it on May 20, 2015.
- FDA terminated it on Aug 17, 2015.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Aurora Products, Inc., of Orange, CT.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- Meat, poultry and egg products are recalled by USDA’s Food Safety and Inspection Service, not FDA, and its recalls aren’t here yet: see fsis.usda.gov.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Food recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.