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Lower risk Food recall · FDA · Published October 3, 2018

Son of Italy Pizza Kits Recalled Due to Room Temperature Cheese Exposure

K.B. Pizza Inc. recalls Son of Italy Twin Pack Cheese Pizza Kits that were left at room temperature for 24 hours, risking bacterial growth. Consumers should check use-by dates and contact the company for details.

🇺🇸 FDA recall #F-0035-2019FoodSon of Italy ›
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Contact the company

Recalling firmK.B. Pizza, Inc.191 Howard St · Franklin, PA 16323-2362
✎ GovInfoNow plain-language explainer

What happened, in plain English

K.B. Pizza Inc. is recalling Son of Italy Twin Pack Cheese Pizza Kits because they were left at room temperature for 24 hours, which could lead to bacterial growth. This affects kits with a use-by date of December 5, 2018, and may pose a food safety risk. Read more at govinfonow.com/recall/18443-son-of-italy-pizza-kits-recalled-due-to-room-temperature.

Source Summary by GovInfoNow · govinfonow.com/recall/18443-son-of-italy-pizza-kits-recalled-due-to-room-temperature · Updated October 6, 2026 · FDA enforcement record: FDA #F-0035-2019

Cite this page

“Son of Italy Pizza Kits Recalled Due to Room Temperature Cheese Exposure.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18443-son-of-italy-pizza-kits-recalled-due-to-room-temperature. Based on FDA recall #F-0035-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0035-2019%22&limit=1).

Why it’s dangerous

The pizza kits were left at room temperature for 24 hours, which can allow bacteria to grow in the cheese packs. This could lead to foodborne illness if the cheese is consumed after the time period.

Who’s affected

Anyone who purchased Son of Italy Twin Pack Cheese Pizza Kits with a use-by date of December 5, 2018, or earlier. People making homemade pizza using these kits are most at risk.

How to tell if you have this one

Check for Son of Italy Twin Pack Cheese Pizza Kits with a use-by date of December 5, 2018 or earlier. The kits are vacuum-packed and come in sets of six per case.

  • Brand
    Son of Italy
  • Category
    Food
FDA recall event · 2 products

All 2 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 III
  • Status
    Terminated
  • Distribution
    All cases were distributed to the following location: Pastores Inc. 6101 E. Lombard St Baltimore, MD 21224
Recall numberProduct, codes & lotsQuantity
F-0035-2019Son of Italy, Twin Pack Cheese Pizza Kit, 39 oz./2 pizzas per kit, Net Wt. 15.5 lbs. 6 pizza kits per case; Use By 12-5-18120 cases
F-0036-2019Son of Italy Pepperoni Pizza Kit ,39 oz./2 pizzas per kit, Net Wt. 15.5 lbs. 6 pizza kits per case; Use By 12-5-18144 cases
Based on the official FDA remedy

What to do — step by step

  1. Check Use-By Date

    Look for the use-by date on the kit or case; if it's December 5, 2018 or earlier, the product is affected.

Where it went and when

Where it was distributed

Distributed in Maryland.

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: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth 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: “All cases were distributed to the following location: Pastores Inc. 6101 E. Lombard St Baltimore, MD 21224” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Oct 3, 201812. FDA classified it Class III: Oct 17, 201823. Published in FDA’s Enforcement Report: Oct 24, 201834. FDA terminated the recall: Jun 18, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class III
  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-0035-2019 (October 3, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0035-2019 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