Moonstruck Chocolate Company Recall: Undeclared milk. - F-0845-2020

🇺🇸 United States

1. February 21, 2020 - Recall initiated
2. March 25, 2020 - Reported by source
3. September 28, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0845-2020

Event ID

85038

Status

Terminated

Classification

Class I

Company

Moonstruck Chocolate Company

Product description

Moonstruck Praline Pecan & Ginger Element Bar in Dark Chocolate, packaged first into a clear poly film that is sealed. The sealed bar is then packed into a cardboard box (1 bar per box) that has label information. Net wt. 3.1 oz. The product SKU number is 312806 and the UPC code is 7 11175 12328 8. The product is also sold in a gold caddy which contains 8 bars. The box has a SKU number of 312806 and the UPC code is 10711175128068. The product label is read in parts: "***INGREDIENTS: Dark Chocolate (unsweetened chocolate, sugar, cocoa butter, soy lecithin {an emulsifier}, vanilla, Caramelized Pecans (pecans, [cocoa butter, salt], sugar, water, spices, Candied Ginger (ginger root, cane sugar)***".

Quantity

1500 bars

Reason

Undeclared milk.

Recall initiation date

February 21, 2020

Report date

March 25, 2020

Classification date

Not published in this source record

Termination date

September 28, 2020

Distribution pattern

nationwide

UPC, lot, and code information

Lot numbers: 1101242, 1101731, 1101734, 1102664, 1102708, 1102754, and 1102914. Best by Dates: 8/11/2020 9/8/2020 9/27/2020 10/3/2020 10/5/2020 8/21/2020 9/19/2020 10/10/2020

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Moonstruck Chocolate Company

Other recalls from Moonstruck Chocolate Company

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of September 28, 2020.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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