“HyVee Turkey Gravy Recall: Undeclared Soy in 12oz Product.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/10047-hyvee-turkey-gravy-recall-undeclared-soy-in-12oz-product. Based on FDA recall #F-0501-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0501-2024%22&limit=1).
The FDA announced on Nov. 20, 2023, that Seneca Foods Corporation is recalling HyVee Turkey Gravy due to undeclared soy. The voluntary Class I recall affects approximately 2,000 jars distributed by Hy-Vee, Inc.
How to tell if you have it
HyVee Turkey Gravy, Net Wt 12 oz (340g)
UPC 0 75450-03608 4
Lot codes A3CG162M and A3CG192M on lid
Best by Jan 28 2025
The hazard
The product poses a risk because it contains undeclared soy, an allergen. The FDA classified this as a Class I recall, indicating a high probability of serious adverse health consequences or death.
Context
GovInfoNow's records show Seneca Foods Corporation has 2 other recalls on record since Oct. 2, 2020. On Oct. 29, 2021, the company recalled pickled beets due to a lack of acidulant. Other recent recalls of similar products include Sliced Korean Halibut with Soy Sauce (July 1, 2026), Good & Gather Sesame Teriyaki Chicken (April 24, 2026), and Troemner Farm Pfeffernusse Cookies (Dec. 19, 2025).
How to tell if you have this one
Check for the UPC code 075450036084 on the product label. The product was distributed by Hy-Vee in West Des Moines, IA.
Brand
HyVee
Product
HyVee Turkey Gravy, Net Wt 12 oz (340g). UPC 0 75450-03608 4. Distributed by Hy-Vee, Inc., West Des Moines, IA 50266
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC code 075450036084 on the gravy container.
Where it went and when
Where it was distributed
Distributed in Iowa.
Listed by the agency
Not listed
FDA distribution: “Product shipped to 2 Hy-Vee Distribution Centers in IA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Iowa.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0501-2024 (November 20, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0501-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.