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EMILIA FOODS SRL Recall: Good and Gather Four Cheese Gnocchi may contain foreign material. - F-0242-2021

United States

TerminatedClass II

Company
EMILIA FOODS SRL
Product
Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Ke…
Recall date
January 15, 2021
Terminated
February 12, 2021
Source
FDA

Reason for recall

Good and Gather Four Cheese Gnocchi may contain foreign material.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Keep Frozen. Needs to be Fully Cooked. UPC 0 85239-10366 1 Product of Italy. Dist by Target Corporation, Minneapolis, MN 55403 Not published in this source record 1199 cases LI0267 BEST if Used By 23 MAR 2022

Distribution

  • Nationwide.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0242-2021
Event ID
87190
Status
Terminated
Classification
Class II
Company
EMILIA FOODS SRL
Product description
Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Keep Frozen. Needs to be Fully Cooked. UPC 0 85239-10366 1 Product of Italy. Dist by Target Corporation, Minneapolis, MN 55403
Quantity
1199 cases
Reason
Good and Gather Four Cheese Gnocchi may contain foreign material.
Recall initiation date
January 15, 2021
Report date
February 3, 2021
Classification date
Not published in this source record
Termination date
February 12, 2021
Distribution pattern
Nationwide.
UPC, lot, and code information
LI0267 BEST if Used By 23 MAR 2022
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

Responsible company: EMILIA FOODS SRL

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:

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 February 12, 2021.

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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