Zingerman's Coffee Company food recall: Zingerman's Peanut Butter Crush Candy Bar net wt 2oz
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97878
- Recall initiated
- Sep 3, 2025
- Classified by FDA
- Nov 10, 2025
- Posted in Enforcement Report
- Nov 19, 2025
- Terminated
- Jan 16, 2026
- Recalling firm
- Zingerman's Coffee Company
- Firm location
- Ann Arbor, MI, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 2
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
Undeclared cashew
Undeclared peanut
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 Sep 3, 2025. FDA classified it 68 days later, on Nov 10, 2025. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: This product was distributed to retailers in Michigan and New York and it reached consumers via retail stores.
Recalled products (2)
H-0178-2026 Class I Terminated
Zingerman's Peanut Butter Crush Candy Bar net wt 2oz UPC 844397005237
Codes / lots: Lot#174250
Quantity: 156 units
H-0179-2026 Class I Terminated
Zingerman's Ca$hew Cow Candy Bar net wt 2oz UPC 844397000157
Codes / lots: Lot#174250
Quantity: 78 units
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 97878
- 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.