Class IITerminated in FDA datasetFeb 17, 2012

Product is 2 oz Peanut Butter. 2 oz pouch labeled in part: "PEANUT BUTTER 2 oz. Pouch***

Recalling firm: Sunshine Peanut Company

Why it was recalled

On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.

Check your package

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

ProductProduct is 2 oz Peanut Butter. 2 oz pouch labeled in part: "PEANUT BUTTER 2 oz. Pouch***Ingredients: Roaster Peanuts, Sugar, Hydrogenated Vegetable Oil, (Rapeseed Cottonseed and/or Soybean Oils), Salt.***Allergen Warning: Contains Peanuts***Sunshine Peanut Company Jacksonville, FL 32204***SP767***" Case Label: "***200/ 2oz Pouch***PEANUT BUTTER***SUNSHINE PEANUT CO.***JACKSONVILLE, FL. 32204***" -- 200/2oz Lot 112312, 112412, 120112 406 shipped to Harvest Farms, Lancaster, CA.

FDA code information

lot code: 112312, 112412, 120112.

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

Full FDA record and distribution details

Original product description

Product is 2 oz Peanut Butter. 2 oz pouch labeled in part: "PEANUT BUTTER 2 oz. Pouch***Ingredients: Roaster Peanuts, Sugar, Hydrogenated Vegetable Oil, (Rapeseed Cottonseed and/or Soybean Oils), Salt.***Allergen Warning: Contains Peanuts***Sunshine Peanut Company Jacksonville, FL 32204***SP767***" Case Label: "***200/ 2oz Pouch***PEANUT BUTTER***SUNSHINE PEANUT CO.***JACKSONVILLE, FL. 32204***" -- 200/2oz Lot 112312, 112412, 120112 406 shipped to Harvest Farms, Lancaster, CA.

Extracted codes and context

TypeCode / valueContext
lot112312lot code: 112312, 112412, 120112.
lot112412lot code: 112312, 112412, 120112.

Recall details

Recall number
F-0117-2013
Event ID
61291
FDA status
Terminated
Initiated
Feb 17, 2012
Reported
Oct 24, 2012
Classified
Oct 16, 2012
Terminated
Nov 1, 2013
Quantity
406 cases
Location
Jacksonville, FL, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Product was distributed to distributors in CA, FL, NJ, and WA.

FDA source record · F-0117-2013

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

Follow official FDA and manufacturer guidance.