RecallHawk
Class I Recall

Nick The Greek Spicy Yogurt Pail, 42lbs pail, UPC 10075365177756, SKU SA000085

Grecian Delight/Kronos

Summary

The FDA issued a Class I for Nick The Greek Spicy Yogurt Pail, 42lbs pail, UPC 10075365177756, SKU SA000085 by Grecian Delight/Kronos. Reason: potential for salmonella.

Details

Source

Food Recall

External ID

F-0379-2025

Action Date

2025-01-15

Status

Terminated

Category

food

Product Description

Nick The Greek Spicy Yogurt Pail, 42lbs pail, UPC 10075365177756, SKU SA000085

Lot/Code Info: Lot 4305

Quantity Affected: 141 - 42 lb. pails

Reason for Recall

potential for salmonella

Distribution

AR CA CO FL GA ID IL IN KS KY LA MD MI MN MO MS NC NJ NV NY OH PA SC TN TX VA WI

Type: Voluntary: Firm initiated

Recall Initiated: 2024-12-02

Company

Grecian Delight/Kronos

Elk Grove Village, IL

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Grecian Delight/Kronos has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Grecian Delight/Kronos) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Grecian Delight/Kronos have FDA actions?

Grecian Delight/Kronos 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-0379-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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