Euphoria Trading Company, LLC. Recall: Potential contamination with Salmonella. Product contains Jif peanut butter.

🇺🇸 United States

1. May 24, 2022 - Recall initiated
2. June 22, 2022 - Reported by source
3. October 18, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1317-2022

Event ID

90319

Status

Terminated

Classification

Class I

Company

Euphoria Trading Company, LLC.

Product description

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.

Quantity

771 Dark Chocolate Peanut Butter Meltaways;

Reason

Potential contamination with Salmonella. Product contains Jif peanut butter.

Recall initiation date

May 24, 2022

Report date

June 22, 2022

Classification date

Not published in this source record

Termination date

October 18, 2022

Distribution pattern

Distributed in Oregon

UPC, lot, and code information

UPC 5046901342; Best By Dates: 10/16/2022 -01/10/2023

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 90319 with 2 other product entries in Public Health Trace.

Responsible company: Euphoria Trading Company, LLC.

Other recalls from Euphoria Trading Company, LLC.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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