Class II Recall

Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil, packaged in 3.4 fl oz (100mL), 8.5 fl oz (250mL), and 17 fl

Summary

The FDA issued a Class II for Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil, packaged in 3.4 fl by LMSI, LLC. Reason: Product contains garlic essential oil not approved for culinary use.

Details

Source

Food Recall

External ID

H-1399-2026

Action Date

2026-10-07

Status

Ongoing

Product Description

Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil, packaged in 3.4 fl oz (100mL), 8.5 fl oz (250mL), and 17 fl oz (500mL) glass bottles, UPC: 799475717185 (on 8.5 fl oz/250mL), 799475717178 (on 17 fl oz/500mL). The 3.4 fl oz/100mL bottles were sold as part of a gift set; the 8.5 fl oz/250mL and 17 fl oz/500mL products were sold individually.

Lot/Code Info: No codes applied

Quantity Affected: Approximately 85 liters

Reason for Recall

Product contains garlic essential oil not approved for culinary use

Distribution

Distributed directly to consumers in CA, FL, IL, KY, MO, NC, OH, OR, TN, TX, VA, WA, and WV

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-29

Company

LMSI, LLC

Montgomery, OH

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 23 food recalls issued in the same week, part of 77 food-related FDA actions this month.

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 (LMSI, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does LMSI, LLC have FDA actions?

This is the only FDA action we have on record for LMSI, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1399-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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