JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units
Summary
The FDA issued a Class I for JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 by Lipari Foods Operating Company, LLC.. Reason: Undeclared milk.
Details
Source
Food Recall
External ID
H-0213-2025
Action Date
2025-07-16
Status
Terminated
Category
food
Product Description
JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
Lot/Code Info: Lot #'s: 28202501A, 29202501A, 23202504A, 14202505A, 15202505A, 03202506A
Quantity Affected: 971 cases
Reason for Recall
Undeclared milk
Distribution
Nationwide in retail stores
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-18
Company
Warren, MI
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 147 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lipari Foods Operating Company, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lipari Foods Operating Company, LLC. have FDA actions?
Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0213-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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