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Lipari Foods, Inc. Recall: JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes. - F-1828-2017

United States

TerminatedClass I

Company
Lipari Foods, Inc.
Product
Premo Ham & Provolone Item # 207851, Net Wt 6 oz; Fresh Gr…
Recall date
February 21, 2017
Terminated
July 18, 2017
Source
FDA

Reason for recall

JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Premo Ham & Provolone Item # 207851, Net Wt 6 oz; Fresh Grab Ham & Provolone Item # 251745, Net Wt 6 oz; Core-Mark Ham & Provolone Item # 568343, Net Wt 6 oz; Not published in this source record 4783 sandwiches Item #: 207851, Lot #s: 05201701, 06201701, 09201701, 10201701, 11201701, 16201701, 18201701, Best by Dates: 1/26/2017 to 2/8/2017; Item # 251745, Lot #s 05201701 and 06201701, Best By Dates: 1/26/2017 and 1/27/2017; Item # 568343, Lot #s: 06201701 and 13201701, Best by Dates: 1/27/2017 and 2/3/2017

Distribution

  • Domestic: MI
  • IL
  • IN
  • KY
  • MD
  • OH
  • PA
  • TN
  • VA
  • WI
  • WV Foreign: None VA/DOD: None

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1828-2017
Event ID
76572
Status
Terminated
Classification
Class I
Company
Lipari Foods, Inc.
Product description
Premo Ham & Provolone Item # 207851, Net Wt 6 oz; Fresh Grab Ham & Provolone Item # 251745, Net Wt 6 oz; Core-Mark Ham & Provolone Item # 568343, Net Wt 6 oz;
Quantity
4783 sandwiches
Reason
JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
Recall initiation date
February 21, 2017
Report date
April 12, 2017
Classification date
Not published in this source record
Termination date
July 18, 2017
Distribution pattern
Domestic: MI, IL, IN, KY, MD, OH, PA, TN, VA, WI, WV Foreign: None VA/DOD: None
UPC, lot, and code information
Item #: 207851, Lot #s: 05201701, 06201701, 09201701, 10201701, 11201701, 16201701, 18201701, Best by Dates: 1/26/2017 to 2/8/2017; Item # 251745, Lot #s 05201701 and 06201701, Best By Dates: 1/26/2017 and 1/27/2017; Item # 568343, Lot #s: 06201701 and 13201701, Best by Dates: 1/27/2017 and 2/3/2017
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 76572 with 7 other product entries in Public Health Trace.

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Thortons Italian & Provolone 12 oz.
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Thortons Italian Footlong 6/12 oz.
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Coffee House Italian Flatbread , Item # 226323 net wt. 6 oz…
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Premo Signature Classic Italian, 1/6 oz.
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Premo Italian Wrap, 1/5 oz.
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Premo Asiago Italian Item # 207919, Net Wt 6 oz; Fresh Gr…
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Premo Turkey & Garlic Mayo Item # 207455, Net wt. 5.5 oz; C…
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

Responsible company: Lipari Foods, Inc.

Other recalls from Lipari Foods, Inc.

FDA Recall United States TerminatedTerminated: October 16, 2018Historical recordClass I

Lipari Foods, Inc.

Product
Premo Brand and Fresh Grab turkey and Swiss submarine sandwi…
Published
August 15, 2018
Distribution
All product was sent to Lipari Foods, Wa…

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FDA Recall United States TerminatedTerminated: January 16, 2018Historical recordClass III

Lipari Foods, Inc.

Product
Sunflower Seeds Honey Roasted, 12oz Tubs & 25lb Bulk
Published
October 4, 2017
Distribution
Domestic Only: MI, FL, SC, OH, KY, WI, M…

View recall →

FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I

Lipari Foods, Inc.

Product
Thortons Italian & Provolone 12 oz.
Published
April 12, 2017
Distribution
Domestic: MI, IL, IN, KY, MD, OH, PA, TN…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Michigan 1
Illinois 1
Indiana 1
Kentucky 1
Maryland 1
Ohio 1
Pennsylvania 1
Tennessee 1
Virginia 1
Wisconsin 1
West Virginia 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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 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 July 18, 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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