RecallHawk
Class II Recall

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

Kabobs Acquisition Inc.

Summary

The FDA issued a Class II for Kabobs The Hors d'oeuvre Specialist TOMATO, BASIL & MASCARPONE ARANCINI 180 COUN by Kabobs Acquisition Inc.. Reason: The firm was notified by their rice supplier that the product may contain small pieces of glass..

Details

Source

Food Recall

External ID

F-1552-2022

Action Date

2022-08-24

Status

Ongoing

Category

food

Product Description

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

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

Quantity Affected: 98cs/3/60 ct trays

Reason for Recall

The firm was notified by their rice supplier that the product may contain small pieces of glass.

Distribution

Product was shipped to the following states: GA, IL, KY, MA, MO, NJ, NY, RI, TX & UT.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-07-14

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Kabobs Acquisition Inc. has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Kabobs Acquisition Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kabobs Acquisition Inc. have FDA actions?

Kabobs Acquisition Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1552-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions