GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE recall
Recalled by Ghirardelli Chocolate Company
The product, as the FDA describes it: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 10lbs (4.54kg) Ingredients: *** nonfat dry milk *** GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 30LB (13.61kg) Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578 UPC (10lbs): 747599662027 UPC (30lbs): 747599418983
Why it was recalled
Potential contamination with Salmonella.
What to do if you have it
Nothing about ghirardelli perfectly premium frappe mix chocolate will look or smell wrong, because the organisms behind this kind of recall leave no trace you can see or taste. Do not cook it to make it safe and do not sample it. Throw it out or return it, then wash anything it touched, including the shelf it sat on and the container beside it.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
---10lbs--- Lot, Best if Used By: S295260A03, 7/31/2027; S395260A03, 7/31/2027. ---30lbs--- Lot, Best if Used By: S195260A03, 5/31/2027; S195261A03, 7/31/2027; S291260A03, 7/31/2027; S295260A03, 7/31/2027; S596260A03, 7/31/2027; S191260A03, 8/31/2027; S291261A03, 8/31/2027.
The details on record
| Recalling company | Ghirardelli Chocolate Company |
|---|---|
| Company location | San Leandro, CA |
| Where it was distributed | 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. |
| How much was recalled | 237 cases (10 lbs/case); 3,488 cases (30 lbs/case) |
| Recall started | April 26, 2026 |
| Published by the FDA | May 27, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | |
| FDA recall number | H-0841-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
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