Guittard Chocolate Company food recall: 72% CACAO CHOCOLATE WITH DATE SUGAR WAFERS Ingredients: Cacao Beans
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 98949
- Recall initiated
- May 5, 2026
- Classified by FDA
- May 29, 2026
- Posted in Enforcement Report
- Jun 10, 2026
- Recalling firm
- Guittard Chocolate Company
- Firm location
- Burlingame, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Letter
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Potential contamination with Salmonella
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on May 5, 2026. FDA classified it 24 days later, on May 29, 2026. Distribution reported by FDA: Domestic Distribution: OH. Foreign Distribution: N/A.
Recalled products (1)
H-0861-2026 Class I Ongoing
72% CACAO CHOCOLATE WITH DATE SUGAR WAFERS Ingredients: Cacao Beans, Organic Date Powder, Organic Cocoa Powder Net Wt 25lb (11.3kg) Made in the USA GUITTARD CHOCOLATE COMPANY Burlingame, CA 94010 Item: 0568C25 UPC: 00071818367654
Codes / lots: Lot code, Best By: 11775A, 12/27/2026; 21775A, 12/27/2026; 31785A, 12/28/2026; 11785A, 12/28/2026; 21785A, 12/28/2026; 22095M, 01/28/2027; 12105M, 01/29/2027; 22105M, 01/29/2027.
Quantity: 2,857 cases (25 lbs/case)
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 98949
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.