Class IITerminatedVoluntary: Firm initiated

House Of Flavors, Inc.: food recall F-0266-2025

House Of Flavors, Inc. of Ludington, MI recalled Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030034940430; 6 retail units per case. Reason: Undeclared soy (soy lecithin). The FDA listed it as Class II in its Enforcement Report dated Dec 18, 2024; distribution: Maryland, Ohio, Pennsylvania, West Virginia.

Record status as published: Terminated (terminated Jan 30, 2025). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030034940430; 6 retail units per case
Product quantity
59 cases
Reason for recall
Undeclared soy (soy lecithin).
Codes, lots and dates on the package
BEST BY MARCH 10, 2026
Distribution pattern
Retail stores in MD, OH, PA, and WV
Recalling firm
House Of Flavors, Inc., Ludington, MI
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
E-Mail

Dates

EventDate
Recall initiated by the firmNov 11, 2024
Classified by the FDADec 11, 2024
Published in the Enforcement ReportDec 18, 2024
TerminatedJan 30, 2025

Other recalls by House Of Flavors, Inc.

  • H-0621-2026 · Mar 18, 2026 · Class I — Undeclared egg
  • H-0384-2026 · Jan 21, 2026 · Class II — Undeclared soy lecithin
  • H-0383-2026 · Jan 21, 2026 · Class II — Undeclared soy lecithin

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0266-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.