Class IITerminatedVoluntary: Firm initiated
LEWIS BAKERIES: food recall H-0319-2025
LEWIS BAKERIES of Evansville, IN recalled Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two… Reason: Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts. The FDA listed it as Class II in its Enforcement Report dated Jul 30, 2025; distribution: Arkansas, Florida, Illinois, Indiana, Kansas, Kentucky, Michigan, Missouri, Ohio, Tennessee, Wisconsin.
Record status as published: Terminated (terminated Aug 18, 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
- Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two splits on top 7/13/2025 - Best By Flexible plastic bag
- Product quantity
- 883 loaves
- Reason for recall
- Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts.
- Codes, lots and dates on the package
- T10 174 010206, T10 174 010306, T10 174 010406, T10 174 020206, T10 174 020306, T10 174 020406, TH10 174 010206, TH10 174 010306, TH10 174 010406, TH10 174 020206, TH10 174 020306, and TH10 174 020406
- Distribution pattern
- Product was distributed to: TN, KS, AR, OH, FL, KY, IN, IL, MI, WI, MO
- Recalling firm
- LEWIS BAKERIES, Evansville, IN
- 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 | Jul 2, 2025 |
| Classified by the FDA | Jul 21, 2025 |
| Published in the Enforcement Report | Jul 30, 2025 |
| Terminated | Aug 18, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0319-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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