"Honey Roasted Peanuts Golden Roast" sold under the Fisher brand and packaged in 14 oz. plastic jars.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1828-2014.
Cases containing 12 x 14 oz. plastic jars of Fisher "Honey Roasted Peanuts Dry Roasted" with a "Best By" date of "5/20/15 N" may contain plastic jars that are mislabeled as Fisher "Peanuts Dry Roasted Golden Roast". Dry roasted honey roasted peanuts contain wheat, which is an allergen, and this allergen is not declared on the dry roasted peanut label.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1828-2014.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact John B. Sanfilippo & Son Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1828-2014.
John B. Sanfilippo & Son Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
John B. Sanfilippo & Son Inc. Recall FAQ
John B. Sanfilippo & Son Inc. is the subject of a seafood safety report: "Honey Roasted Peanuts Golden Roast" sold under the Fisher brand and packaged in 14 oz. plastic jars.. The notice was published on March 20, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 945 units are potentially affected.