Class I Recall

White Cheddar Seasoning packed in the following sizes and configurations: 1. Net Wt. 1.2 oz (34g) Distributed by: Fi

Summary

The FDA issued a Class I for White Cheddar Seasoning packed in the following sizes and configurations: 1. by Jonco Industries. Reason: Products were made with recalled California Dairies milk powder due to Salmonella..

Details

Source

Food Recall

External ID

H-0953-2026

Action Date

2026-06-24

Status

Ongoing

Product Description

White Cheddar Seasoning packed in the following sizes and configurations: 1. Net Wt. 1.2 oz (34g) Distributed by: Fireworks Popcorn, Division of Jonco Industries, Milwaukee, WI 53218. Sold in a Fireworks Popcorn, Natural American Popcorn Popping & Toppings gift set. Contains: 3 popcorns & 3 popcorns seasonings. 2. Net Wt. 1.6 oz. (45g) UPC 7 36659-26501 8. Distributed by: Fireworks Popcorn, Division of Jonco Industries, Milwaukee, WI 53218. Sold at West Allis Cheese and Sausage retail store. 3. Net Wt 0.7 oz (19g) Williams Sonoma, Not for Retail Sale. Sold in a Williams Sonoma branded Popcorn Sampler Gift Box. Set includes 2 popcorns, oil, seasoning and salt.

Lot/Code Info: 1. Lot# 088594-5-1 2. Lot# 088594-7-1 3. Lot# 088594-2-1

Quantity Affected: 1407 jars total

Reason for Recall

Products were made with recalled California Dairies milk powder due to Salmonella.

Distribution

MS, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-04

Company

Jonco Industries

Milwaukee, WI

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 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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

How often does Jonco Industries have FDA actions?

This is the only FDA action we have on record for Jonco Industries in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0953-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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