Food Recall Check
Class I · High risk Terminated Initiated Sep 3, 2025 (13 months ago)

Zingerman's Peanut Butter Crush Candy Bar recall

Recalled by Zingerman's Coffee Company · Ann Arbor, MI, United States

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

Why it was recalled

Undeclared cashew

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

Zingerman's Peanut Butter Crush Candy Bar net wt 2oz UPC 844397005237

Quantity: 156 units

Food: Peanut butter 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.

Lot#174250

Where it was sold

Michigan New York

FDA's distribution note: This product was distributed to retailers in Michigan and New York and it reached consumers via retail stores.

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
Zingerman's Coffee Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 3, 2025
In FDA report of
Nov 19, 2025
Terminated
Jan 16, 2026
FDA recall number
H-0178-2026 · event 97878
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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