Euphoria Trading Company, LLC. Recall: 70% Dark Chocolate Buttons products are recalled due to undeclared soy lecithin.

🇺🇸 United States

1. June 12, 2019 - Recall initiated
2. July 3, 2019 - Reported by source
3. September 13, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1522-2019

Event ID

83106

Status

Terminated

Classification

Class II

Company

Euphoria Trading Company, LLC.

Product description

70% Dark Chocolate Buttons packaged in cellophane bags, zip bags (plastic bag with Ziploc closure), a bulk bin in the factory store. Net wt. 3 oz., 8 oz., 16 oz., 3 lbs (48 oz.) UPC on 3 oz. bag: 0 50469 05423 UPC on 8 oz. bag: 0 50469 05424 or 0 50469 05497 UPC on 16 oz. bag: 0 50469 05117 or 0 50469 05495 UPC on 48 oz. bag: 0 50469 05493 The retail labels are read in parts: "***70% Dark Chocolate Buttons *** Ingredients: chocolate liquor, sugar, chocolate liquor processed in alkali, cocoa butter, vanilla *** May contain milk & soy. Processed on shared equipment with items that may contain peanuts, tree nuts, wheat, and egg***". The CASE labels are read in parts: "***Button Extreme Dark 70%***

Quantity

301 bags total (3oz. = 84; 8oz = 97; 16oz = 66; 3lbs = 54)

Reason

70% Dark Chocolate Buttons products are recalled due to undeclared soy lecithin.

Recall initiation date

June 12, 2019

Report date

July 3, 2019

Classification date

Not published in this source record

Termination date

September 13, 2019

Distribution pattern

distributed in Oregon

UPC, lot, and code information

Best If Used By: 12/5/2020 Lot Code: 34018AMBAA

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.

• Email
• X / Twitter
• Facebook