Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported September 21, 2016
Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label reading in part "Dollywood Candy Kitchen". UPC code 4 9000 503302
Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta.
Rucker's Makin Batch Candies, Inc. recalled Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label readi… - a critical-severity action.
Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label readi… was recalled by Rucker's Makin Batch Candies, Inc. in September 21, 2016. Reason: Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta.. Check the official notice for the remedy. Verify recall #F-2222-2016 with the FDA Food before acting.
The recall
Rucker's Makin Batch Candies, Inc. issued this critical-severity FDA Food recall-Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta..
- Critical
- severity level
- Class I
- classification
- September 21, 2016
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2222-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2222-2016) was formally reported on September 21, 2016, with the manufacturer initiating the action on June 7, 2016. It is classified under Critical severity (Class I), with a current status of Terminated. Rucker's Makin Batch Candies, Inc. is listed as the recalling firm, operating out of Bridgeport, IL. Federal records list the affected scope as 389 bags, 9 ounces per bag.
The documented reason for this recall is: Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta. Distribution data in the federal record shows the product reached: The firm shipped this product to one retail facility. The retail facility is Dollywood Theme Park, 1130 Wagner Drive, Sevierville, TN 37862. No foreign Consignees.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
389 bags, 9 ounces per bag
Related Recalls
6
2 from same agency
Product description
Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label reading in part "Dollywood Candy Kitchen". UPC code 4 9000 503302
Reason for recall
Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-2222-2016 |
| Date reported | September 21, 2016 |
| Date initiated | June 7, 2016 |
| Recalling firm | Rucker's Makin Batch Candies, Inc. |
| Firm location | Bridgeport, IL |
| Affected scope | 389 bags, 9 ounces per bag |
| Distribution | The firm shipped this product to one retail facility. The retail facility is Dollywood Theme Park, 1130 Wagner Drive, Sevierville, TN 37862. No foreign Consignees. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-2222-2016) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Dollywood Cajun Mix packaged in a clear 9 ounce plastic bag with grey sticker label reading in part "Dollywood Candy Kitchen". UPC code 4 9000 503302. Recalled by Rucker's Makin Batch Candies, Inc.. Units affected: 389 bags, 9 ounces per bag.
Why was this product recalled? ▼
Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 21, 2016. Severity: Critical. Recall number: F-2222-2016.
Where was the recalled product distributed? ▼
Distribution: The firm shipped this product to one retail facility. The retail facility is Dollywood Theme Park, 1130 Wagner Drive, Sevierville, TN 37862. No foreign Consignees..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2222-2016) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 21, 2016. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.