Kabobs Truffle Arancini Recalled for Potential Glass Contamination
Kabobs Acquisition Inc. is recalling Truffle Arancini with Wild Mushrooms due to potential glass pieces in the rice. The product was distributed to multiple states.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall for glass contamination in a food product. While glass contamination poses a risk of injury, no illnesses or injuries have been reported in the source text, per the rubric criterion for risk-of-harm products without reported injury.
Plain-English summary
Kabobs Acquisition Inc. is recalling Kabobs The Hors d'oeuvre Specialist Truffle Arancini with Wild Mushrooms (180 count) due to potential glass contamination. The firm was notified by their rice supplier that the product may contain small pieces of glass.
The recalled product, identified by Product Code K8142 and Lot numbers PM22F21, PM22F22, PM22F29, and PM22G12, was distributed to Georgia, Illinois, Kentucky, Massachusetts, Missouri, New Jersey, New York, Rhode Island, Texas, and Utah.
Consumers who have purchased this product should not consume it. Those with concerns about their health should contact their healthcare provider. Retailers should remove the product from shelves and contact their distributor for return instructions.
The recalled product
- Product
- 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
- Manufacturer
- Kabobs Acquisition Inc.
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Product Code K8142
- Lot #: PM22F21
- PM22F22
- PM22F29 & PM22G12.
Distribution
Part of a larger recall action
This product is one of 2 recalled by Kabobs Acquisition Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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