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…
United States
TerminatedClass I
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.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Premo Signature Classic Italian, 1/6 oz. | Not published in this source record | 429 sandwiches | Premo Signature Classic Italian, 1/6 oz., Item No: 519111 Product #: 519111, Lot No. 04201701 06201701 09201701 11201701 13201701 16201701 Sell By Dates: 1/17/2017 1/19/2017 1/22/2017 1/24/2017 1/26/2017 1/29/2017 UPC: 612510090916 |
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
FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I
Responsible company: Lipari Foods, Inc.
FDA Recall United States TerminatedTerminated: October 16, 2018Historical recordClass I
FDA Recall United States TerminatedTerminated: January 16, 2018Historical recordClass III
FDA Recall United States TerminatedTerminated: July 18, 2017Historical recordClass I
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.
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.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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.
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This record is preserved as published by FDA, as of July 18, 2017.
Status as reported: Terminated.
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