RecallHawk
Class I Recall

GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry mi

Ghirardelli Chocolate Company

Summary

The FDA issued a Class I for GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2o by Ghirardelli Chocolate Company. Reason: Potential contamination with Salmonella..

Details

Source

Food Recall

External ID

H-0842-2026

Action Date

2026-05-27

Status

Ongoing

Category

food

Product Description

GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599662003

Lot/Code Info: Lot, Best if Used By: S397261, 2/28/2027; S397262, 4/30/2027; S397263, 6/30/2027.

Quantity Affected: 309 cases (6-50oz units/case); 1,854 units

Reason for Recall

Potential contamination with Salmonella.

Distribution

U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-26

Company

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

Ghirardelli Chocolate Company has 10 FDA actions in our database, including 10 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 (Ghirardelli Chocolate Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ghirardelli Chocolate Company have FDA actions?

Ghirardelli Chocolate Company has 10 FDA actions in our database, including 10 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0842-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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