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Grace Kennedy Foods USA LLC Recall: La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes. - F-1808-2017

United States

TerminatedClass II

Company
Grace Kennedy Foods USA LLC
Product
La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Distribute…
Recall date
February 20, 2017
Terminated
March 5, 2019
Source
FDA

Reason for recall

La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Distributed: by La Fe Foods Moonachne, NJ 07074 UPC Not published in this source record 2005 cases lote 225 16 vence 12 08 18

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1808-2017
Event ID
76550
Status
Terminated
Classification
Class II
Company
Grace Kennedy Foods USA LLC
Product description
La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Distributed: by La Fe Foods Moonachne, NJ 07074 UPC
Quantity
2005 cases
Reason
La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes.
Recall initiation date
February 20, 2017
Report date
April 5, 2017
Classification date
Not published in this source record
Termination date
March 5, 2019
Distribution pattern
Nationwide
UPC, lot, and code information
lote 225 16 vence 12 08 18
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

Responsible company: Grace Kennedy Foods USA LLC

Other recalls from Grace Kennedy Foods USA LLC

FDA Recall United States TerminatedTerminated: March 25, 2022Historical recordClass II

Grace Kennedy Foods USA LLC

Product
La Fe Brand Frozen Peppers and Onions 16 oz bags.
Published
April 7, 2021
Distribution
Distributed to retail stores in CT, DE,…

View recall →

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 March 5, 2019.

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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