FDA Recall United States Terminated Historical recordClass I
Theo Chocolate Inc
- Product
- Theo Chocolate Salted Almond 70% Dark Chocolate bars are wra…
- Published
- September 21, 2016
- Distribution
- distributed in AZ, CA, CO, CT, FL, GA, I…
Public Health Trace republishes official recall, outbreak, and surveillance data from CDC, FDA, USDA, WHO, and other public sources. It is an independent information service, not a medical provider, and not a substitute for professional medical advice or your local public health department's own guidance.
Please review the following before continuing:
Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared milk.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Sea Salt 70% Dark Chocolate 3 oz. bars, wrapped in foil and paper wrapper, brand Theo Chocolate, UPC 8 74492 00325 8. The Sea Salt 70% Dark Chocolate 3 oz. bar's label is read in part: "***Sea Salt 70% Dark Chocolate *** Ingredients: Cocoa Beans, Cane Sugar, Sea Salt, Ground Vanilla Bean *** Allergy Information: Manufactured on shared equipment with products containing milk, eggs, wheat, peanuts & tree nuts ***". These Sea Salt 70% Dark Chocolate 3 oz. bars are packed in the MASTER CASE that is labeled as: Salted Toffee 55% Dark Chocolate, 3092529 BEST BY 1/2020, Time Stamp 05:00 - 08:15, UPC 20874492003818. These Sea Salt 70% Dark Chocolate are packed in the INNER CASE that is labeled as: Salted Toffee 55% Dark Chocolate, 3092529 BEST BY 1/2020, Time Stamp 05:00 - 08:15, UPC 10874492003811. ***The Salted Toffee 55% Dark Chocolate individual 3 oz bars (UPC 8 74492 00381 4) are labeled CORRECTLY and not subject to this recall. | 20874492003818 | 29,364 bars | Lot code 3092529 Best-By date of 1/2020 |
Responsible company: Theo Chocolate Inc
FDA Recall United States Terminated Historical recordClass I
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.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
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.
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.
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.
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.