Lower riskFood recall · FDA · Published November 11, 2024
House Of Flavors Butter Pecan Reduced Fat Butter Recall: Undeclared Soy
House Of Flavors recalls 6 units of Butter Pecan Reduced Fat 48 fl oz butter with undeclared soy lecithin. Consumers should check UPC 030034940430 for affected products.
“House Of Flavors Butter Pecan Reduced Fat Butter Recall: Undeclared Soy.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/8618-house-of-flavors-butter-pecan-reduced-fat-butter-recall-undeclared. Based on FDA recall #F-0266-2025 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0266-2025%22&limit=1).
House Of Flavors, Inc. voluntarily recalled Giant Eagle churned Butter Pecan Reduced Fat ice cream due to undeclared soy, the FDA said on Nov. 11, 2024. The product contains soy lecithin, posing an allergy risk to consumers.
The product contains undeclared soy lecithin, which may cause allergic reactions in individuals with soy allergies. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show House Of Flavors, Inc. has six other recalls on file since March 4, 2014. Recent brand recalls include a Feb. 26, 2026, vanilla ice cream recall for undeclared egg and a Dec. 12, 2025, banana pudding ice cream recall for undeclared soy lecithin. Other recent recalls of similar products include BEF Foods Park St. Deli Macaroni & Cheese (March 23, 2026), Prospector Popcorn (April 28, 2026), and ASUKAR TETAS Cherry Milkshake Popsicle (March 11, 2026).
How to tell if you have this one
Check for the UPC 030034940430 on the product label. The butter was sold in Giant Eagle stores with a best-by date of March 10, 2026.
Brand
House Of Flavors
Product
Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030034940430; 6 retail units per case
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 030034940430 on the butter package to confirm it's affected.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “Retail stores in MD, OH, PA, and WV” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Maryland, Ohio, Pennsylvania, West Virginia.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
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-0266-2025 (November 11, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0266-2025 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.