Hickory Harvest FOODS Rucker's Cajun Mix 25 lb. bag in a box INGREDIENTS: Cajun Sesame Sticks***soybean oil***Sunflower Kernels, Hot & S...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0319-2017.
The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0319-2017.
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 Ohio Hickory Harvest Brand Products 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-0319-2017.
Ohio Hickory Harvest Brand Products 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.
Ohio Hickory Harvest Brand Products Inc. Recall FAQ
Ohio Hickory Harvest Brand Products Inc. is the subject of a food safety report: Hickory Harvest FOODS Rucker's Cajun Mix 25 lb. bag in a box INGREDIENTS: Cajun Sesame Sticks***soybean oil***Sunflower Kernels, Hot & S.... The notice was published on May 4, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 685 units are potentially affected.