Premo Ham & Provolone (Lipari Foods) – Cheese Contamination (2017)
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 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;
Brand
Lipari Foods, Inc.
Lot Codes / Batch Numbers
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
Products Sold
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
Lipari Foods, Inc. is recalling Premo Ham & Provolone Item # 207851, Net Wt 6 oz; Fresh Grab Ham & Provolone Item # 251745, Net W due to 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 . 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
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.
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
IL, IN, KY, MD, MI, OH, PA, TN, VA, WV, WI
Page updated: Jan 6, 2026