Class IIITerminated in FDA datasetRecall initiated Dec 22, 2025

Willy Pete's Chocolates brand Almond Despair; Dark Chocolate with Coconuts, Almonds, & Carolina…

Recalling firm: Willy Pete's Chocolate Company LLC

Why it was recalled

Almonds are not declared in the ingredient statement. Almond is included in description of product on front label.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 25, 2026.

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ProductWilly Pete's Chocolates brand Almond Despair; Dark Chocolate with Coconuts, Almonds, & Carolina Reapers; Ingredients: Sugar, Vegetable Oil, (Palm Kernel Oil & Hydrogentated Palm Kernel Oil), Cocoa Powder (processed with Alkali), Soy Lecithin (An Emulsifier), Whey Powder (Milk) & Salt. Coconut, Sugar, Water Propylene Glycol (Sustains Freshness), Salt, Sodium Metabisulfite (Preserves Whiteness). Macadamia nuts & Carolina Reaper Powder; Contains Milk and Soy. Tree Nuts. May contain traces of peanuts; UPC: 0 987261 5

FDA code information

No additional coding. UPC Codes: 09872615

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Full FDA record and distribution details

Original product description

Willy Pete's Chocolates brand Almond Despair; Dark Chocolate with Coconuts, Almonds, & Carolina Reapers; Ingredients: Sugar, Vegetable Oil, (Palm Kernel Oil & Hydrogentated Palm Kernel Oil), Cocoa Powder (processed with Alkali), Soy Lecithin (An Emulsifier), Whey Powder (Milk) & Salt. Coconut, Sugar, Water Propylene Glycol (Sustains Freshness), Salt, Sodium Metabisulfite (Preserves Whiteness). Macadamia nuts & Carolina Reaper Powder; Contains Milk and Soy. Tree Nuts. May contain traces of peanuts; UPC: 0 987261 5

Original FDA recall reason

Almonds are not declared in the ingredient statement. Almond is included in description of product on front label.

Recall details

Recall number
H-0484-2026
Event ID
98209
FDA status
Terminated
Initiated
Dec 22, 2025
Reported
Feb 11, 2026
Classified
Feb 5, 2026
Terminated
Feb 25, 2026
Quantity
54 units
Location
Harwinton, CT, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

MA, SC, CT

FDA source record · H-0484-2026

Data updated September 16, 2026. View official FDA data ↗

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