Deskins Candies, Peanut Butter Pinwheel ,16 oz., Plastic Shell, 12-16oz. packages per case.
Summary
The FDA issued a Class I for Deskins Candies, Peanut Butter Pinwheel ,16 oz., Plastic Shell, 12-16oz. package by Deskins Wholesale, LLC. Reason: Products were made with peanut butter contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-1309-2022
Action Date
2022-06-22
Status
Terminated
Category
food
Product Description
Deskins Candies, Peanut Butter Pinwheel ,16 oz., Plastic Shell, 12-16oz. packages per case.
Lot/Code Info: Peanut Butter Pinwheel 733980123147
Quantity Affected: 181 Cases
Reason for Recall
Products were made with peanut butter contaminated with Salmonella.
Distribution
The products were distributed domestically, WV, VA, and NC .
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-22
Company
Bluefield, WV
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 175 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Deskins Wholesale, LLC has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Deskins Wholesale, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Deskins Wholesale, LLC have FDA actions?
Deskins Wholesale, LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1309-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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