Class IITerminated in FDA datasetJun 12, 2019

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.

Recalling firm: Euphoria Trading Company, LLC.

Why it was recalled

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

Check the codes ↓

The exact product

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%***

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

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

TypeCode / valueContext
best by12/5/2020Best If Used By: 12/5/2020 Lot Code: 34018AMBAA
lot34018AMBAABest If Used By: 12/5/2020 Lot Code: 34018AMBAA

Recall details

Recall number
F-1522-2019
Event ID
83106
FDA status
Terminated
Initiated
Jun 12, 2019
Reported
Jul 3, 2019
Classified
Jun 27, 2019
Terminated
Sep 13, 2019
Quantity
301 bags total (3oz. = 84; 8oz = 97; 16oz = 66; 3lbs = 54)
Location
Eugene, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

distributed in Oregon

FDA source record · F-1522-2019

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.