Poppies International INC Recall: Products may be contaminated with Listeria monocytogenes - F-1141-2018

🇺🇸 United States

1. March 21, 2018 - Recall initiated
2. April 18, 2018 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1141-2018

Event ID

79607

Status

Completed

Classification

Class II

Company

Poppies International INC

Product description

GFS Belgian Mini Chocolate Topped Eclairs, Keep Frozen, Net Wt . 700 g.; Signature Select Belgian Style Mini Eclairs, Keep Frozen, 420 g; Delizza Patisserie Belgian Custard Cream Mini Eclairs, 420 g.

Quantity

Delizza: 9664 cases; GFS: 3819 cases; Signature Select: 5400 cases

Reason

Products may be contaminated with Listeria monocytogenes

Recall initiation date

March 21, 2018

Report date

April 18, 2018

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Nationwide

UPC, lot, and code information

GFS Product UPC 093901859372, Lot code: L1D1018, Best Before 09/06/19; Signature Select UPC 021130085460, Lot code: L1G1018, Best Before 09/07/19; Delizza UPC 676670001069; Lot code: L1M1018, Best Before 09/09/19

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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: Poppies International INC

Other recalls from Poppies International INC

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 "Completed." 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.

Status as reported: Completed.

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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