FDA Recall United States Terminated Historical 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…
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.
United States
TerminatedClass I
- Company
- Lipari Foods, Inc.
- Product
- Premo Turkey & Garlic Mayo Item # 207455, Net wt. 5.5 oz; C…
- 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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Premo Turkey & Garlic Mayo Item # 207455, Net wt. 5.5 oz; Core-Mark Turkey & Garlic Mayo Item # 568207, Net wt. 5.5 oz; Fresh Grab Turkey & Provolone with Garlic Mayo Item # 455956, Net wt. 5.5 oz | Not published in this source record | 2495 sandwiches | Item #: 207455, Lot #s: 05201701; 06201701; 09201701; 10201701; 11201701; 13201701, Best By Dates: 1/20/2017 to 2/4/2017; Item # 568207, Lot #s 06201701 and 13201701, Best By Dates: 1/25/2017 to 2/1/2017; Item # 455956, Lot #s: 05021701, 06201701, 10201701, 17201701 |
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-1827-2017
- Event ID
- 76572
- Status
- Terminated
- Classification
- Class I
- Company
- Lipari Foods, Inc.
- Product description
- Premo Turkey & Garlic Mayo Item # 207455, Net wt. 5.5 oz; Core-Mark Turkey & Garlic Mayo Item # 568207, Net wt. 5.5 oz; Fresh Grab Turkey & Provolone with Garlic Mayo Item # 455956, Net wt. 5.5 oz
- Quantity
- 2495 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 #: 207455, Lot #s: 05201701; 06201701; 09201701; 10201701; 11201701; 13201701, Best By Dates: 1/20/2017 to 2/4/2017; Item # 568207, Lot #s 06201701 and 13201701, Best By Dates: 1/25/2017 to 2/1/2017; Item # 455956, Lot #s: 05021701, 06201701, 10201701, 17201701
- 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 Terminated Historical 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…
FDA Recall United States Terminated Historical 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…
FDA Recall United States Terminated Historical 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…
FDA Recall United States Terminated Historical 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…
FDA Recall United States Terminated Historical 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…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods, Inc.
- Product
- Premo Ham & Provolone Item # 207851, Net Wt 6 oz; Fresh Gr…
- Published
- April 12, 2017
- Distribution
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN…
Responsible company: Lipari Foods, Inc.
Other recalls from Lipari Foods, Inc.
FDA Recall United States Terminated Historical 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…
FDA Recall United States Terminated Historical 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…
FDA Recall United States Terminated Historical 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…
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.
| 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.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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.
