GOULIBEUR Recall: This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated. - F-1590-2017

🇺🇸 United States

1. January 27, 2017 - Recall initiated
2. March 22, 2017 - Reported by source
3. October 16, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1590-2017

Event ID

76444

Status

Terminated

Classification

Class II

Company

GOULIBEUR

Product description

Goulibeur- Cube tin box Life in Paris, containing mini heart-shaped pure butter shortbreads Net weight 4.23 oz

Quantity

800 units

Reason

This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated.

Recall initiation date

January 27, 2017

Report date

March 22, 2017

Classification date

Not published in this source record

Termination date

October 16, 2017

Distribution pattern

U.S.: Maryland

UPC, lot, and code information

Batch number : 16490 Best-by date : 08/15/2017

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 76444 with 5 other product entries in Public Health Trace.

Responsible company: GOULIBEUR

Other recalls from GOULIBEUR

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 II mean?

FDA classifies this recall as Class II. 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 October 16, 2017.

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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