Cajun Hot Mix 6 OZ. packaged in clear plastic bags with sticker label. This product has multiple brands. All brands are under the same UP...
⚠ 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-1740-2016.
Sunflower kernels in this product are contaminated with Listeria Monocytogenes per the original supplier, SunOpta.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1740-2016.
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 Rucker's Wholesale & Service Co., 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-1740-2016.
Rucker's Wholesale & Service Co., 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.
Rucker's Wholesale & Service Co., Inc. Recall FAQ
Rucker's Wholesale & Service Co., Inc. is the subject of a food safety report: Cajun Hot Mix 6 OZ. packaged in clear plastic bags with sticker label. This product has multiple brands. All brands are under the same UP.... The notice was published on June 8, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 3,915 units are potentially affected.