Food Recall Check
Class I · High risk Terminated Initiated May 22, 2022 (4 years ago)

Deskins Candies Peanut Butter Pinwheel recall

Recalled by Deskins Wholesale, LLC · Bluefield, WV, United States

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

Why it was recalled

Products were made with peanut butter contaminated with Salmonella.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

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

Deskins Candies, Peanut Butter Pinwheel ,16 oz., Plastic Shell, 12-16oz. packages per case.

Quantity: 181 Cases

Food: Peanut butter Chocolate & candy

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.

Peanut Butter Pinwheel 733980123147

Where it was sold

North Carolina Virginia West Virginia

FDA's distribution note: The products were distributed domestically, WV, VA, and NC .

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
Deskins Wholesale, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 22, 2022
In FDA report of
Jun 22, 2022
Terminated
Sep 19, 2023
FDA recall number
F-1309-2022 · event 90321
Official record
FDA enforcement report search

Also recalled with it (3 more products)

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

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