Peanut Butter Classic Truffles are peanut butter ganache centers dipped in milk chocolate and topped with salt flakes. N
Summary
The FDA issued a Class I for Peanut Butter Classic Truffles are peanut butter ganache centers dipped in milk by Euphoria Trading Company, LLC.. Reason: Potential contamination with Salmonella. Product contains Jif peanut butter..
Details
Source
Food Recall
External ID
F-1316-2022
Action Date
2022-06-22
Status
Terminated
Category
food
Product Description
Peanut Butter Classic Truffles are peanut butter ganache centers dipped in milk chocolate and topped with salt flakes. Net wt. is approximately 1.45oz. Peanut Butter Classic Truffles sold over display case or distributed in 12pc package, Euphoria Chocolate brand. UPC 5046907226. Peanut Butter Classic Truffles are also distributed in 64 piece boxes and they are not meant for retail sale and do not have the firm name and address listed. The product is put into display cases and will be packed at the time of sale. UPC 5046907225.
Lot/Code Info: Best By Dates: 03/15/2022 - 06/20/2022
Quantity Affected: 1840 individual pieces Truffles
Reason for Recall
Potential contamination with Salmonella. Product contains Jif peanut butter.
Distribution
Distributed in Oregon
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-24
Company
Eugene, OR
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.
Euphoria Trading Company, LLC. has 3 FDA actions in our database, including 3 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 (Euphoria Trading Company, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Euphoria Trading Company, LLC. have FDA actions?
Euphoria Trading Company, LLC. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1316-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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