Food Recall Check
Class I · High risk Terminated Initiated Dec 20, 2025 (10 months ago)

Fran s PureBar Almondmilk Chocolate 46% Madagascar Plant-Based recall

Recalled by Fran's Chocolates Ltd · Seattle, WA, United States

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

Why it was recalled

undeclared hazelnut.

Undeclared allergen: Tree nuts

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Fran s PureBar Almondmilk Chocolate 46% Madagascar Plant-Based, net wt. 1.1oz, UPC 7 49668 24280 2. Ingredients: Sugar, cocoa butter, cocoa beans, almonds, sunflower lecithin, vanilla extract. May contain traces of milk, peanuts and sesame. Fran's Chocolates, Ltd. Seattle, WA 98108.

Quantity: 112 units

Food: Chocolate & candy

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.

None

Where it was sold

Colorado Massachusetts Nevada Washington

FDA's distribution note: Distributed in CO, MA, NV, WA and online at www.frans.com

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. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Fran's Chocolates Ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 20, 2025
In FDA report of
Jan 21, 2026
Terminated
Jan 29, 2026
FDA recall number
H-0399-2026 · event 98195
Official record
FDA enforcement report search

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