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Lower risk Food recall · FDA · Published October 16, 2018

Hy-Vee Spinach Tomatoes Mozzarella Potatoes Recall: Listeria and Salmonella Risk

Hy-Vee recalls spinach, tomato, mozzarella twice baked potatoes potentially contaminated with Listeria monocytogenes and Salmonella. Products with lot numbers 16012-18281 sold by October 22, 2018.

🇺🇸 FDA recall #F-0347-2019FoodHy-Vee ›
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Recalling firmD & D Foods, Inc.9425 N 48th St · Omaha, NE 68152-1557
✎ GovInfoNow plain-language explainer

What happened, in plain English

Hy-Vee is recalling spinach, tomato, mozzarella twice baked potatoes that may contain Listeria monocytogenes or Salmonella. This could cause foodborne illness if eaten. Read more at govinfonow.com/recall/18286-hy-vee-spinach-tomatoes-mozzarella-potatoes-recall-listeria-and-salmonella.

Source Summary by GovInfoNow · govinfonow.com/recall/18286-hy-vee-spinach-tomatoes-mozzarella-potatoes-recall-listeria-and-salmonella · Updated October 5, 2026 · FDA enforcement record: FDA #F-0347-2019

Cite this page

“Hy-Vee Spinach Tomatoes Mozzarella Potatoes Recall: Listeria and Salmonella Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18286-hy-vee-spinach-tomatoes-mozzarella-potatoes-recall-listeria-and-salmonella. Based on FDA recall #F-0347-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0347-2019%22&limit=1).

Why it’s dangerous

The products may be contaminated with Listeria monocytogenes or Salmonella bacteria. These bacteria can cause foodborne illness, especially in people with weakened immune systems.

Who’s affected

Anyone who purchased Hy-Vee spinach, tomato, mozzarella twice baked potatoes with lot numbers 16012 through 18281 before October 22, 2018. People with weakened immune systems are at higher risk.

How to tell if you have this one

Check the lot number on the product label, which ranges from 16012 to 18281. Products were sold by October 22, 2018, with a net weight of 5 ounces wrapped in clear plastic.

  • Brand
    Hy-Vee
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for lot numbers 16012 through 18281 on the product label.

Where it went and when

Where it was distributed

Distributed in 7 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: yesSDIowa: yesIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: yesNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: yesKSArkansas: 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: “Distributed to a distributor in Iowa and further distributed to retail stores in Iowa, Illinois, Kansas, Minnesota, Missouri, Nebraska, and South Dakota.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota.

Recall timeline

FDA terminated this recall 22 days after the firm started it.

1. Firm started the recall: Oct 16, 201812. FDA classified it Class II: Oct 31, 201823. Published in FDA’s Enforcement Report: Nov 7, 201834. FDA terminated the recall: Nov 7, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  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-0347-2019 (October 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0347-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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