Milk Chocolate Covered Peanut Butter Meltaways 8oz. Item code: K120M
Summary
The FDA issued a Class I for Milk Chocolate Covered Peanut Butter Meltaways 8oz. Item code: K120M by Cargill Cocoa and Chocolate Inc. Reason: Possible contamination with Salmonella.
Details
Source
Food Recall
External ID
F-1289-2022
Action Date
2022-06-22
Status
Terminated
Category
food
Product Description
Milk Chocolate Covered Peanut Butter Meltaways 8oz. Item code: K120M
Lot/Code Info: Lot 220222AA with Best if Used by Date of 4/22/2022 Lot 220218AG with Best if Used by Date of 4/18/2022 Lot 220215AE with Best if Used by Date of 4/15/2022
Quantity Affected: 795 boxes Total
Reason for Recall
Possible contamination with Salmonella
Distribution
Retail store in PA. Consumers in PA, SC, NC, VA, MD, DE, MA, WA, IN, IA, GA, IL, NJ, and NY
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-23
Company
Lititz, PA
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.
Cargill Cocoa and Chocolate Inc has 7 FDA actions in our database, including 7 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 (Cargill Cocoa and Chocolate Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cargill Cocoa and Chocolate Inc have FDA actions?
Cargill Cocoa and Chocolate Inc has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1289-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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