Recall record at a glance
| Official record | F-0113-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Sunshine Peanut Company |
| Report date | Oct 24, 2012 |
| Recall initiation date | Feb 17, 2012 |
| Quantity | 72 - 35lb pails; 1344 - 6/5lb Tubs. |
| Location | Jacksonville, FL, United States |
Official product description
Sunny Boy Peanut Butter. Product is labeled in part: 6/5 lb tubs- "SunnyBoy Creamy PEANUT BUTTER***Net Wt. 5lb. (2.27KG)***INGREDIENTS: Peanuts, Dextrose, Contains less than 2% of the following: Salt, Partially Hydrogenated Oil (Rapeseed Cottonseed And/Or Mono-Diglycerides)***Allergen Statement: CONTAINS PEANUTS***Sunshine Peanut Company Tampa, FL 33637*** -- Driscoll product 1,344 cases Lot 111912 & 112012. 35 lb pail labeled in part: ""SunnyBoy Creamy PEANUT BUTTER***Net Wt. 35lb. (15.89KG)***INGREDIENTS: Peanuts, Dextrose, Contains less than 2% of the following: Salt, Partially Hydrogenated Oil (Rapeseed Cottonseed And/Or Mono-Diglycerides)***Allergen Statement: CONTAINS PEANUTS***Sunshine Peanut Company Tampa, FL 33637*** -- South Bay Correctional Facility, South Bay, FL (Good Source) 72 Pails Lot 112412.
Why the product 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.
Distribution information
Product was distributed to distributors in CA, FL, NJ, and WA.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.