Recall Register

Food recall: Dark Chocolate Coffee Beans, Natural Dark Chocolate Coffee Beans

Class II FDA enforcement event 78578. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

JLM Manufacturing LLC started this food recall on 16 Nov 2017. The firm address in the FDA record is in Warren, MI. FDA put the recall in Class II. FDA event 78578 has 5 product records. The first FDA enforcement report date is 20 Dec 2017. The record gives the status Terminated, with the termination date 30 Mar 2018.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Sole customer is Lipari located in MI who further distributed to multiple states including: Alabama, Florida, Illinois, Indiana, Iowa, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Nebraska,…

Recalling firm

JLM Manufacturing LLC, Warren, MI.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

5 product records in the event.

FDA event 78578: product records
Recall numberProductQuantityClassStatusReport date
F-0494-2018Dark Chocolate Coffee Beans, Natural Dark Chocolate Coffee BeansUnknownClass IITerminated20 Dec 2017
F-0495-2018Dark Chocolate Raisins, Natural Dark Chocolate RaisinsUnknownClass IITerminated20 Dec 2017
F-0496-2018Dark Chocolate Almond Bark, 12/8oz.UnknownClass IITerminated20 Dec 2017
F-0497-2018Natural Dark Chocolate CranberriesUnknownClass IITerminated20 Dec 2017
F-0498-2018Dark Chocolate Almonds, Natural Dark Chocolate Almonds, 12/7 oz., and 12/12 oz.UnknownClass IITerminated20 Dec 2017

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Food events that started in 2017
599
Share of these events in Class II
52%
Product records in this event
5Median of the firm: 5
Events of the firm on the register
2

Other events of the firm

Other FDA enforcement events of JLM Manufacturing LLC
InitiatedProduct (first record)TypeClassRecords
3 Oct 2022JLM Sesame Sticks Mix in clear plastic 11oz. tub UPC 094776081646 12 retail units per caseFoodClass II2

Official channels

Cite this page

Recall Register. FDA enforcement event 78578. https://recallregister.com/fda/ii/78578/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Sole customer is Lipari located in MI who further distributed to multiple states including: Alabama, Florida, Illinois, Indiana, Iowa, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Nebraska,…
What quantity of product is in FDA event 78578?
The event has 5 product records. The first record gives this quantity: Unknown
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2017 have the same class?
52% of the 599 food events that started in 2017 are in Class II.