FDA recall record

Guittard Chocolate Company 72% CACAO CHOCOLATE WITH DATE SUGAR WAFERS Ingredients: Cacao recall — FDA H-0861-2026

Potential contamination with Salmonella

Class Iclassification
H-0861-2026official record ID
Jun 10, 2026report date

Recall record at a glance

Official recordH-0861-2026
CategoryFood Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmGuittard Chocolate Company
Report dateJun 10, 2026
Recall initiation dateMay 5, 2026
Quantity2,857 cases (25 lbs/case)
LocationBurlingame, CA, United States

Official product description

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

Why the product was recalled

Potential contamination with Salmonella

Distribution information

Domestic Distribution: OH. Foreign Distribution: N/A.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.