Dark Chocolate Peanut Butter Meltaways (Euphoria) – Salmonella Contamination (2022)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dark Chocolate Peanut Butter Meltaways are rectangular bars with the filling consisting of crunchy peanut butter and milk chocolate and are then dipped in dark chocolate. Net wt. is approximately 1.25oz. UPC 5046901342. Each box consists of 70 pieces 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.
Brand
Euphoria Trading Company, LLC.
Lot Codes / Batch Numbers
Best By Dates: 10/16/2022 -01/10/2023
Products Sold
Best By Dates: 10/16/2022 -01/10/2023
Euphoria Trading Company, LLC. is recalling Dark Chocolate Peanut Butter Meltaways are rectangular bars with the filling consisting of crunchy p due to Potential contamination with Salmonella. Product contains Jif peanut butter.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential contamination with Salmonella. Product contains Jif peanut butter.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, OR
Page updated: Jan 6, 2026