Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label reading in part "Dollywood Candy Kitchen". UPC code 4...
⚠ 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-2222-2016.
Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2222-2016.
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 Makin Batch Candies, 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-2222-2016.
Rucker's Makin Batch Candies, 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 Makin Batch Candies, Inc. Recall FAQ
Rucker's Makin Batch Candies, Inc. is the subject of a snacks & candy safety report: Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label reading in part "Dollywood Candy Kitchen". UPC code 4.... The notice was published on June 7, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 389 units are potentially affected.