Artisan Style 1/2 Loaf recall
Recalled by Lewis Bakeries · Evansville, IN, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
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.
Undeclared allergen: Tree nuts
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your 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
Where it was sold
Arkansas Florida Illinois Indiana Kansas Kentucky Michigan Missouri Ohio Tennessee Wisconsin
FDA's distribution note: Product was distributed to: TN, KS, AR, OH, FL, KY, IN, IL, MI, WI, MO
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Lewis Bakeries
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 2, 2025
- In FDA report of
- Jul 30, 2025
- Terminated
- Aug 18, 2025
- FDA recall number
- H-0319-2025 · event 97198
- Official record
- FDA enforcement report search