LEWIS BAKERIES 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.
United States
TerminatedClass II
- Company
- LEWIS BAKERIES
- Product
- Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/…
- Recall date
- July 2, 2025
- Terminated
- August 18, 2025
- Source
- FDA
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 883 loaves | 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
- Product was distributed to: TN
- KS
- AR
- OH
- FL
- KY
- IN
- IL
- MI
- WI
- MO
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0319-2025
- Event ID
- 97198
- Status
- Terminated
- Classification
- Class II
- Company
- LEWIS BAKERIES
- Product description
- 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
- Quantity
- 883 loaves
- 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.
- Recall initiation date
- July 2, 2025
- Report date
- July 30, 2025
- Classification date
- Not published in this source record
- Termination date
- August 18, 2025
- Distribution pattern
- Product was distributed to: TN, KS, AR, OH, FL, KY, IN, IL, MI, WI, MO
- UPC, lot, and code information
- 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: LEWIS BAKERIES
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Tennessee | 1 |
| Kansas | 1 |
| Arkansas | 1 |
| Ohio | 1 |
| Florida | 1 |
| Kentucky | 1 |
| Indiana | 1 |
| Illinois | 1 |
| Michigan | 1 |
| Wisconsin | 1 |
| Missouri | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
