FDA recall, , High risk
French Broad Chocolate Bette's Bake Sale Bonbon Assortment
The bonbon assortment may contain undeclared walnuts, which can cause serious allergic reactions in people with tree nut allergies.
Recall ended Sep 1, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor chocolates (bonbons). Consumers relying on the printed materials could mistakenly consume a nut-containing bonbon.
4 photos
What to do
If a code on your package is listed below:
- Consumers with a tree nut allergy who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product.
- Consumers with questions may contact Customer Service at support@
frenchbroadchocolates.com or 828.252.4181, between 9am and 5pm EST.
Is yours affected?
Affected if its lot code is listed.
Bette’s Bake Sale 6 piece
- Size
- 2.5oz
- Lot code
- Batch 260414 Jun 29 2026
- Batch 260417 Jun 30 2026
Bette’s Bake Sale 12 piece
- Size
- 5oz
- Lot code
- Batch 260414 Jun 22 2026
- Batch 260417 Jun 30 2026
Bette’s Bake Sale 24 piece
- Size
- 10 oz
- Lot code
- Batch 260414 Jun 29 2026
- Batch 260417 Jun 30 2026
Recall details
- Company began the recall
- Sold in
- 40 states and DC
- Alabama
- Arizona
- Arkansas
- California
- Colorado
- Connecticut
- District of Columbia
- Florida
- Georgia
- Illinois
- Indiana
- Iowa
- Kentucky
- Louisiana
- Maryland
- Massachusetts
- Michigan
- Minnesota
- Mississippi
- Missouri
- Montana
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- New York
- North Carolina
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Vermont
- Virginia
- Washington
- West Virginia
- Wisconsin
- Company
- French Broad Chocolate FactoryAsheville, North Carolina
- Hazard
- Undeclared tree nut
- Risk
High risk
There is a reasonable chance that eating it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98806
- Recall number
- H-0712-2026
- Quantity recalled
- 34/2.5oz boxes, 400/5oz boxes, 53/10oz boxes
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall · Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Recall ended
Summary updated
