Food recall

Kabobs Acquisition Inc. recall: Kabobs The Hors d'oeuvre Specialist TOMATO, BASIL & MASCARPONE ARANCINI 180 COUNT Prepared by

Kabobs Acquisition Inc., of Lake City, GA, recalled Kabobs The Hors d'oeuvre Specialist TOMATO, BASIL & MASCARPONE ARANCINI 180 COUNT Prepared by and 1 other product. The FDA's reason: “The firm was notified by their rice supplier that the product may contain small pieces of glass.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on July 14, 2022, and the FDA first listed it in its Enforcement Report of August 24, 2022. The recall is still going on.

How serious

Class II

It could cause temporary or minor harm

Why

Metal, plastic, glass or other objects

Status

Ongoing

The recall

Company
Kabobs Acquisition Inc. (Lake City, GA)
Reason, in FDA's words
“The firm was notified by their rice supplier that the product may contain small pieces of glass.”
Where it was sold
Product was shipped to the following states: GA, IL, KY, MA, MO, NJ, NY, RI, TX & UT.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
90612

The 2 products recalled

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

  • F-1552-2022 Class II

    Kabobs The Hors d'oeuvre Specialist TOMATO, BASIL & MASCARPONE ARANCINI 180 COUNT Prepared by: Kabobs, Inc., 5423 North Lake Dr., Lake City, GA 30260

    Codes: Product Code: K8143, Lot #: PM22F23, PM22F30 & PM22G13.

    Quantity: 98cs/3/60 ct trays

  • F-1553-2022 Class II

    Kabobs The Hors d'oeuvre Specialist TRUFFLE ARANCINI WITH WILD MUSHROOMS 180 COUNT Prepared by: Kabobs, Inc., 5423 North Lake Dr., Lake City, GA 30260

    Codes: Product Code K8142, Lot #: PM22F21, PM22F22, PM22F29 & PM22G12.

    Quantity: 112cs/3/60 ct trays

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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 August 24, 2022.

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.