CLASS I Food recall · Reported 16 Jul 2025 · FDA Enforcement Report

JLM Manufacturing Dark Chocolate Nonpareils recalled

Lipari Foods Operating Company is recalling JLM Manufacturing Dark Chocolate Nonpareils, distributed nationwide in the US. The recall was initiated on 18 Jun 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #'s: 28202501A, 29202501A, 23202504A, 14202505A, 15202505A, 03202506A
Quantity recalled971 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0213-2025
FDA event ID
97120
Recalling firm
Lipari Foods Operating Company, Warren, MI
Classification
Class I
Status
Terminated
Recall initiated
18 Jun 2025
FDA classified
7 Jul 2025
Reported
16 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Chocolate

Timeline

18 Jun 2025Recall initiated by company
7 Jul 2025Classified by FDA+19 days
16 Jul 2025Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared milk

Product as listed by the FDA

JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case

Where it was distributed

Nationwide in retail stores

Nationwide

Questions about this recall

Why was it recalled?

Undeclared milk

Which lots are affected?

Lot #'s: 28202501A, 29202501A, 23202504A, 14202505A, 15202505A, 03202506A

Where was it sold?

Nationwide in retail stores

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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