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Lower risk Food recall · FDA · Published July 22, 2017

Hy-Vee Cheese Pizza Recall: Soy Not Listed on Ingredients

Hy-Vee recalls 16" Thin Crust Cheese Pizza with soy lecithin not declared on ingredients list. Consumers should check UPC 288942 611991 for affected products.

🇺🇸 FDA recall #F-3392-2017FoodHy-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 its 16-inch thin crust cheese pizza because soy lecithin is present but not listed on the ingredients or contains statement. This could affect people with soy allergies who might react to the hidden soy ingredient. Read more at govinfonow.com/recall/20636-hy-vee-cheese-pizza-recall-soy-not-listed-on-ingredients.

Source Summary by GovInfoNow · govinfonow.com/recall/20636-hy-vee-cheese-pizza-recall-soy-not-listed-on-ingredients · Updated October 7, 2026 · FDA enforcement record: FDA #F-3392-2017

Cite this page

“Hy-Vee Cheese Pizza Recall: Soy Not Listed on Ingredients.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20636-hy-vee-cheese-pizza-recall-soy-not-listed-on-ingredients. Based on FDA recall #F-3392-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3392-2017%22&limit=1).

Why it’s dangerous

Soy lecithin is a common soy-derived ingredient that can cause allergic reactions in sensitive individuals. The product does not list soy on its ingredients or contains statement, which is required by labeling laws for allergens.

Who’s affected

People with soy allergies who consume this pizza may experience allergic reactions. The recall affects specific Hy-Vee cheese pizzas sold in West Des Moines, Iowa.

How to tell if you have this one

Check for the UPC 288942 611991 on the product label. The pizza was sold in West Des Moines, Iowa, with best-by dates from April 23, 2017 to July 26, 2017.

  • Brand
    Hy-Vee
  • Product
    Hy-Vee, Cheese Pizza, 16'' Thin Crust, UPC 288942 611991, Net Wt. 29 oz (1 lb 13 oz) 1.81 lb (822 g), West Des Moines
  • Category
    Food
FDA recall event · 4 products

All 4 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 II
  • Status
    Terminated
  • Distribution
    The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.
Recall numberProduct, codes & lotsQuantity
F-3389-2017Hy-Vee, Cheese Pizza, 12'' Traditional Crust, UPC 288900 908996, Net Wt. 26 oz (1 lb 10 oz) 1.62 lb (737 g), West Des Moines, IA; Best if Used by Dates: 04-23-2017 thru 07-26-2017471/4 pizzas/cases
F-3390-2017Hy-Vee, Cheese Pizza, 16'' Traditional Crust, UPC 288928 611991, Net Wt. 47 oz (2 lb 15 oz) 2.94 lb (1.332 kg), West Des Moines, IA; Best if Used by Dates: 04-23-2017 thru 07-26-2017419/4 pizzas/cases
F-3391-2017Hy-Vee, Cheese Pizza, 12'' Thin Crust, UPC 288914 908999, Net Wt. 17 oz (1 lb 1 oz) 1.06 lb (482 g), West Des Moines, IA; Best if Used by Dates: 04-23-2017 thru 07-26-2017182/4 pizzas/cases
F-3392-2017Hy-Vee, Cheese Pizza, 16'' Thin Crust, UPC 288942 611991, Net Wt. 29 oz (1 lb 13 oz) 1.81 lb (822 g), West Des Moines, IA; Best if Used by Dates: 04-23-2017 thru 07-26-2017119/4 pizzas/cases
Based on the official FDA remedy

What to do — step by step

  1. Check Ingredients

    Look for soy lecithin on the ingredients list or check the contains statement for soy.

How this recall unfolded

Recall timeline

FDA terminated this recall 47 days after the firm started it.

1. Firm started the recall: Jul 22, 201712. FDA classified it Class II: Aug 18, 201723. Published in FDA’s Enforcement Report: Aug 30, 201734. FDA terminated the recall: Sep 7, 201742017
  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-3392-2017 (July 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3392-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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