Ghirardelli Perfectly Premium Frappe Mix Vanilla recall

Recalled by Ghirardelli Chocolate Company · San Leandro, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Potential contamination with Salmonella.

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA NET WT 48oz (3lbs) 1.36kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599621055

Quantity: 489 cases (6-48oz units/case); 2,934 units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot, Best if Used By: S495260, 3/31/2027; S495261, 6/30/2027; S594262, 7/31/2027.

Where it was sold

Alaska Arizona California Florida Georgia Idaho Illinois Indiana Kentucky Maryland Maine Minnesota North Carolina New Jersey Nevada New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin

FDA's distribution note: 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.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall.

Recalling firm: Ghirardelli Chocolate Company
Initiated by: Voluntary: Firm initiated
Recall initiated: Apr 26, 2026
In FDA report of: May 27, 2026
FDA recall number: H-0843-2026 · event 98851
Official record: FDA enforcement report search

Also recalled with it (9 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class I · High risk Ongoing Salmonella Apr 26, 2026