Food recall

MUNK PACK INC recall: Munk Pack Keto Nut and Seed Dark Chocolate Sea Salt Bar

MUNK PACK INC, of Greenwich, CT, recalled Munk Pack Keto Nut and Seed Dark Chocolate Sea Salt Bar and 3 other products. The FDA's reason: “Product may contain undeclared milk.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on December 16, 2019, and the FDA first listed it in its Enforcement Report of February 12, 2020. 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 July 29, 2020

The recall

Company
MUNK PACK INC (Greenwich, CT)
Reason, in FDA's words
“Product may contain undeclared milk”
Where it was sold
NY, FL
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
84517

The 4 products recalled

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

  • F-0590-2020 Class II

    Munk Pack Keto Nut and Seed Dark Chocolate Sea Salt Bar, 35 g, individual unit

    Codes: NOV052020 and NOV062020 UPC: 853787005764

    Quantity: N/A

  • F-0591-2020 Class II

    Munk Pack Peanut Butter Dark Chocolate Nut & Seed Bar, 35 g, individual unit

    Codes: NOV052020 and NOV062020 UPC: 853787005917

    Quantity: N/A

  • F-0592-2020 Class II

    Munk Pack Coconut Cocoa Chip Keto Granola Bar, 4 pack, 128 g

    Codes: NOV042020 UPC: 853787005849

    Quantity: N/A

  • F-0593-2020 Class II

    Munk Pack Almond Butter Cocoa Chip Keto Granola Bar, 4 pack, 128 g

    Codes: NOV042020 UPC: 853787005481

    Quantity: 449 (total all four products, awaiting breakdown)

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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 February 12, 2020.

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.