Recall record at a glance
| Official record | F-1300-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Theo Chocolate Inc. |
| Report date | Apr 17, 2019 |
| Recall initiation date | Mar 27, 2019 |
| Quantity | 29,364 bars |
| Location | Seattle, WA, United States |
Official product description
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.
Why the product was recalled
Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared milk.
Distribution information
nationwide
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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