Food recall

Mindo Chocolate Makers LLC recall: Mindo COFFEE TOFFEE CHOCOLATE BAR

Mindo Chocolate Makers LLC, of Dexter, MI, recalled Mindo COFFEE TOFFEE CHOCOLATE BAR. The FDA's reason: “Undeclared milk.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on March 11, 2021, and the FDA first listed it in its Enforcement Report of March 31, 2021. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Allergen not on the label

Status

Terminated

Closed September 1, 2021

The recall

Company
Mindo Chocolate Makers LLC (Dexter, MI)
Reason, in FDA's words
“Undeclared milk”
Where it was sold
Retailers in MI and online
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
87543

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0426-2021 Class II

    Mindo COFFEE TOFFEE CHOCOLATE BAR, 75 gram / 2.65oz UPC code 805993900527. Also sold in 12 count and 6 count cartons

    Codes: Lot Numbers 190310 through 210310

    Quantity: 2187 bars

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of March 31, 2021.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.