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Lower risk Food recall · FDA · Published October 4, 2018

Ukrop's Cuban Style Sub Recall: Listeria Risk from Country Ham Equipment

Ukrop's recalls Cuban Style Subs (8.3 oz) due to potential Listeria contamination from country ham processing equipment. Consumers should check UPC 72251525152 for affected products.

🇺🇸 FDA recall #F-0609-2019FoodUkrop's ›
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Contact the company

Recalling firmUkrop's Homestyle Foods, LLC600 Southlake Blvd Ste A · North Chesterfield, VA 23236-3956
✎ GovInfoNow plain-language explainer

What happened, in plain English

Ukrop's is recalling Cuban Style Subs (8.3 oz) because they may have been contaminated with Listeria from equipment used for country ham. This poses a risk of serious illness if consumed. Read more at govinfonow.com/recall/18427-ukrop-s-cuban-style-sub-recall-listeria-risk-from-country.

Source Summary by GovInfoNow · govinfonow.com/recall/18427-ukrop-s-cuban-style-sub-recall-listeria-risk-from-country · Updated October 6, 2026 · FDA enforcement record: FDA #F-0609-2019

Cite this page

“Ukrop's Cuban Style Sub Recall: Listeria Risk from Country Ham Equipment.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18427-ukrop-s-cuban-style-sub-recall-listeria-risk-from-country. Based on FDA recall #F-0609-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0609-2019%22&limit=1).

Why it’s dangerous

The products may have been exposed to equipment that processed country ham for a previous Listeria recall. Listeria can cause serious illness, but the risk here is low due to the specific recall context.

Who’s affected

Owners of Ukrop's Cuban Style Subs (8.3 oz) with UPC 72251525152 are affected. Those with the product are at risk if they consume it.

How to tell if you have this one

Check for the UPC 72251525152 on the product label. The product is a 8.3 oz (235g) Cuban Style Sub from Ukrop's Homestyle Foods.

  • Brand
    Ukrop's
  • Product
    Ukrop's Cuban Style Sub, NET WT 8.3 OZ (235g), UPC 72251525152
  • Category
    Food
FDA recall event · 12 products

All 12 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    Product was shipped to 5 different states: Virginia, West Virginia, Kentucky, Ohio, Tennessee. Retailer List The Kroger Co.  VA, WV, TN, KY, OH Harris Teeter  VA only Publix  VA only Hudson News  VA only Ukrops Catering  VA only
Recall numberProduct, codes & lotsQuantity
F-0605-2019Ukrop's Black Forest Ham & Provolone Sub NET WT 7.8 OZ (221g) UPC 72251525153; 1251532702 Packages
F-0606-2019Ukrop's Country Ham on Petite Biscuits 8CT, NET WT 14 OZ (397g), UPC 72251524271; 12427188 Packages
F-0607-2019Ukrop's Country Ham on Petite Party Rolls 20CT, NET WT 17.7 OZ (1.11lb/502g), UPC 72251524487; 12448735 Packages
F-0608-2019Ukrop's Country Ham on White House Rolls 12CT, 2CT, 6CT, NET WT 23.3 OZ (1.46lb/660g), NET WT 3.9 OZ (110g), NET WT 11.6 OZ (330g), UPC 72251524485, 72251524479,72251524486; 124485 124479 1244863595 Packages
F-0609-2019Ukrop's Cuban Style Sub, NET WT 8.3 OZ (235g), UPC 72251525152; 1251522600 Packages
F-0610-2019Ukrop's Ham on Petite Party Rolls 20CT, NET WT 21.8 OZ (1.36lb/618g) , UPC 72251524094; 12409444 Packages
F-0611-2019Ukrop's Ham on White House Rolls 12CT, NET WT 26.9 OZ (1.68lb/762g) UPC 72251525154 ,; 12515467 Packages
F-0612-2019Ukrop's Honey Ham & Swiss on White House Rolls 2CT, NET WT 5.5 OZ (155g) UPC 72251525075; 1250755786 Packages
F-0613-2019Ukrop's Honey Ham & Turkey on White House Rolls 4CT, NET WT 11 OZ (311g), UPC 72251525071; 1250713400 Packages
F-0614-2019Ukrop's Honey Turkey & Cheddar on White House Rolls 2CT, NET WT 5.5 OZ (155g), UPC 72251525074; 1257046152 Packages
F-0615-2019Ukrop's Italian Style Sub , NET WT 8.2 OZ (232g) UPC 72251525151; 1251516602 Packages
F-0616-2019Ukrop's Roasted Turkey & Colby Jack Sub, NET WT 8.3 OZ (235g), UPC 72251525142; 1251424668 Packages
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 72251525152 on the 8.3 oz Cuban Style Sub package.

Where it went and when

Where it was distributed

Distributed in 5 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Product was shipped to 5 different states: Virginia, West Virginia, Kentucky, Ohio, Tennessee. Retailer List The Kroger Co.  VA, WV, TN, KY, OH Harris Teeter  VA only Publix  VA only Hudson News  VA only Ukrops Catering  VA only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Kentucky, Ohio, Tennessee, Virginia, West Virginia.

Recall timeline

FDA terminated this recall 21 months after the firm started it.

1. Firm started the recall: Oct 4, 201812. FDA classified it Class I: Nov 13, 201823. Published in FDA’s Enforcement Report: Nov 21, 201834. FDA terminated the recall: Jun 26, 2020420182020
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0609-2019 (October 4, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0609-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA