Cajun Hot Mix recall

Recalled by Rucker's Wholesale & Service Co., Inc. · Bridgeport, IL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Sunflower kernels in this product are contaminated with Listeria Monocytogenes per the original supplier, SunOpta.

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

CAJUN HOT MIX 8 OZ. packaged in a clear plastic bag with sticky label under the UPC number 052545022689, and several brand names, including ATWOOD'S RANCH & HOME, BASS PRO SHOP'S UNCLE BUCK'S, BIG R STORE'S, CABELA'S CLASSIC'S, CABELA'S OUTFITTER CLASSIC, FARM & HOME SUPPLY, F & S TRADING, JAYS SPORTING GOODS, MOO'D FOOD /MURDOCHS, and RURAL KING

Quantity: 24,112 bags

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 date 071316 to 051617

Where it was sold

Nationwide.

FDA's distribution note: 70 retail stores nationwide. Product was also shipped to canada firms. please see attached spread sheet for a full list of customers.

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 Wholesale & Service Co., Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Jun 8, 2016
In FDA report of: Jul 27, 2016
Terminated: Feb 27, 2018
FDA recall number: F-1744-2016 · event 74375
Official record: FDA enforcement report search

Also recalled with it (7 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class I · High risk Terminated Listeria Jun 8, 2016