Turkey Swiss Submarine Sandwiches (Lipari Foods) – Product Safety (2018)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches, 4/6 oz, and 18/6 oz.
Brand
Lipari Foods, Inc.
Lot Codes / Batch Numbers
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
Products Sold
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
Lipari Foods, Inc. is recalling Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches, 4/6 oz, and 18/6 oz. due to Lipari Foods, LLC has issued a voluntary recall of Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches produced and packaged by sister co. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
MI
Page updated: Jan 6, 2026