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…
Lipari Foods, Inc. Recall: Lipari Foods, LLC has issued a voluntary recall of Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches produced and packaged by sister company JLM due to potential contamination of Listeria monocytogenes
United States
TerminatedClass I
- Company
- Lipari Foods, Inc.
- Product
- Premo Brand and Fresh Grab turkey and Swiss submarine sandwi…
- Recall date
- July 27, 2018
- Terminated
- October 16, 2018
- Source
- FDA
Reason for recall
Lipari Foods, LLC has issued a voluntary recall of Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches produced and packaged by sister company JLM due to potential contamination of Listeria monocytogenes
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches, 4/6 oz, and 18/6 oz. | Not published in this source record | 1258 units | Brand Product Lipari Product # Weight Sell By Date Lot # UPC Premo Brand, Turkey & Swiss Sub, Product # 915537, Weight: 4/6 OZ, Sell By: 08/06/2018, Lot # 17201807, UPC: 612510001042; and Fresh Grab Turkey & Swiss Sub, Product #: 251694, Weight: 18/6 OZ, Sell By: 08/06/2018, Lot #: 17201807, and UPC: 612510001042 |
Distribution
- All product was sent to Lipari Foods
- Warren
- MI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1760-2018
- Event ID
- 80658
- Status
- Terminated
- Classification
- Class I
- Company
- Lipari Foods, Inc.
- Product description
- Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches, 4/6 oz, and 18/6 oz.
- Quantity
- 1258 units
- Reason
- Lipari Foods, LLC has issued a voluntary recall of Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches produced and packaged by sister company JLM due to potential contamination of Listeria monocytogenes
- Recall initiation date
- July 27, 2018
- Report date
- August 15, 2018
- Classification date
- Not published in this source record
- Termination date
- October 16, 2018
- Distribution pattern
- All product was sent to Lipari Foods, Warren, MI
- UPC, lot, and code information
- Brand Product Lipari Product # Weight Sell By Date Lot # UPC Premo Brand, Turkey & Swiss Sub, Product # 915537, Weight: 4/6 OZ, Sell By: 08/06/2018, Lot # 17201807, UPC: 612510001042; and Fresh Grab Turkey & Swiss Sub, Product #: 251694, Weight: 18/6 OZ, Sell By: 08/06/2018, Lot #: 17201807, and UPC: 612510001042
- 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
Responsible company: Lipari Foods, Inc.
Other recalls from Lipari Foods, Inc.
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…
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…
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 |
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.
