Lipari Foods Operating Company, LLC. food recall: JLM Manufacturing Dark Chocolate Nonpareils
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97120
- Recall initiated
- Jun 18, 2025
- Classified by FDA
- Jul 7, 2025
- Posted in Enforcement Report
- Jul 16, 2025
- Terminated
- Aug 19, 2025
- Recalling firm
- Lipari Foods Operating Company, LLC.
- Firm location
- Warren, 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
- 1
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 milk
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 Jun 18, 2025. FDA classified it 19 days later, on Jul 7, 2025. Distribution reported by FDA: Nationwide in retail stores Lipari Foods Operating Company, LLC. has 13 recalls in our records.
Recalled products (1)
H-0213-2025 Class I Terminated
JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
Codes / lots: Lot #'s: 28202501A, 29202501A, 23202504A, 14202505A, 15202505A, 03202506A
Quantity: 971 cases
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 97120
- 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.