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

Hy-Vee Spring Pasta Salad Recall: Salmonella Risk from 2018 Products

Hy-Vee recalls spring pasta salad products from June 22, 2018 to August 3, 2018 due to potential Salmonella contamination. Consumers should check product dates and containers for affected items.

🇺🇸 FDA recall #F-1930-2018FoodHy-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 spring pasta salad products that may contain Salmonella Sandiego or Salmonella enterica subspecies IIIb. This recall is due to an outbreak of illnesses linked to these products. Read more at govinfonow.com/recall/18965-hy-vee-spring-pasta-salad-recall-salmonella-risk-from-2018.

Source Summary by GovInfoNow · govinfonow.com/recall/18965-hy-vee-spring-pasta-salad-recall-salmonella-risk-from-2018 · Updated October 6, 2026 · FDA enforcement record: FDA #F-1930-2018

Cite this page

“Hy-Vee Spring Pasta Salad Recall: Salmonella Risk from 2018 Products.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18965-hy-vee-spring-pasta-salad-recall-salmonella-risk-from-2018. Based on FDA recall #F-1930-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1930-2018%22&limit=1).

Why it’s dangerous

Salmonella bacteria can cause food poisoning with symptoms like diarrhea, fever, and abdominal cramps. The outbreak is linked to specific Hy-Vee pasta salad products from the specified time period.

Who’s affected

Anyone who purchased Hy-Vee Spring Pasta Salad between June 22, 2018 and August 3, 2018. People who ate the product and experienced illness should contact their healthcare provider.

How to tell if you have this one

Check for Hy-Vee Spring Pasta Salad in plastic tubs with lids (16 oz or 48 oz) or labeled cases from June 22, 2018 to August 3, 2018. Also look for clear plastic unlabeled deli containers from that time.

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

What to do — step by step

  1. Check Product Date

    Look for expiration dates between June 22, 2018 and August 3, 2018 on the packaging.

  2. Discard Affected Products

    If you have products from the specified dates, discard them immediately to avoid potential illness.

Where it went and when

Where it was distributed

Distributed in 8 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: 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: “To Hy-Vee retail stores in IA, IL, KS, MN, MO, NE, SD, and WI.” 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, Wisconsin.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Jul 16, 201812. Published in FDA’s Enforcement Report: Aug 15, 201823. FDA classified it Class I: Aug 30, 201834. FDA terminated the recall: Sep 14, 201842018
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  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-1930-2018 (July 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1930-2018 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