Class IITerminatedVoluntary: Firm initiated
Harvey Investments LLC / The Baking Group: food recall F-0700-2025
Harvey Investments LLC / The Baking Group of Dallas, TX recalled Brioche Bread Loaf and Hamburger buns packaged in brown box and labeled as follows: 1. Ben E. Keith Co. Dense Brioche… Reason: Undeclared allergens (soy, milk) and Yellow #5. The FDA listed it as Class II in its Enforcement Report dated Apr 16, 2025; distribution: Texas.
Record status as published: Terminated (terminated Sep 11, 2026). 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
- Brioche Bread Loaf and Hamburger buns packaged in brown box and labeled as follows: 1. Ben E. Keith Co. Dense Brioche Pullman Loaf, 33 oz. 7 Count, Case Wt. 15 lbs. Product Code: 654203. The Bakery Group, 9106 Sovereign Row, Dallas, TX 75247. GTIN: 00038597654203 2. Ben E. Keith Co. 4.5" Brioche HB Buns. 3oz. 48 count, Case Wt. 10 lbs. Product Code: 54500. The Bakery Group, 9106 Sovereign Row, Dallas, TX 75247. GTIN: 00038597654203. 3. Rodeo Goat Casa Linda Brioche Pullman Loaf, 33 oz. 7 count, Case Wt. 15 lbs. Product Code: 654203. The Bakery Group, 9106 Sovereign Row, Dallas, TX 75247. GTIN: 00038597654203.
- Product quantity
- 733 cases
- Reason for recall
- Undeclared allergens (soy, milk) and Yellow #5
- Codes, lots and dates on the package
- No identifying lot numbers. Product Code: 654203.
- Distribution pattern
- TX
- Recalling firm
- Harvey Investments LLC / The Baking Group, Dallas, TX
- 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
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 19, 2025 |
| Classified by the FDA | Apr 9, 2025 |
| Published in the Enforcement Report | Apr 16, 2025 |
| Terminated | Sep 11, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0700-2025 (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.