Dollywood Cajun Mix packaged in a clear
Reason Cajun Mix containing sunflower kernels are contaminated with Listeria Monocytogenes per the supplier SunOpta.
Dollywood" Dollywood sweet and salty trail mix packaged in an recall
Recalled by Rucker's Makin Batch Candies, Inc. · Bridgeport, IL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Sunflower kernels received from the supplier and subsequently used in the trail mix bag may be contaminated with Listeria Monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Labeled in part "Dollywood". Dollywood sweet and salty trail mix packaged in an 11 oz clear plastic bag with a grey sticker label containing red lettering. UPC 490000503272
Quantity: 240 bags, 11 oz per bag.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Best by dates of 11-22-2016 and 1-6-2017
Where it was sold
FDA's distribution note: The firm shipped to one direct account.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Rucker's Makin Batch Candies, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 6, 2016
- In FDA report of
- Sep 28, 2016
- Terminated
- Dec 21, 2018
- FDA recall number
- F-2378-2016 · event 74101
- Official record
- FDA enforcement report search