Recalls / Class II
Class IIF-0248-2023
Product
Sanders Dark Chocolate Sea Salt Caramels: UPC 0-35900-26442-9 36OZ Tub UPC 0-35900-27488-6 28OZ Tub UPC 0-35900-26442-9 2/36OZ Tub UPC 0-35900-30167-4 7OZ Pouch UPC 0-35900-30852-9 7OZ Gift Box UPC 0-35900-30987-8 18OZ Tub UPC 0-35900-30988-5 9OZ Pouch UPC 0-35900-30969-4 18OZ Tub UPC 0-35900-31045-4 14oz Gift Box
- Type
- Food
- Affected lot / code info
- Best By dates: 10/14/2023,10/15/2023,10/16/2023,10/18/2023,10/19/2023,10/25/2023,10/28/2023,10/29/2023,11/02/2023,12/07/2023,12/08/2023,12/09/2023,12/10/2023,12/11/2023,12/22/2023,12/23/2023,12/24/2023,12/26/2023,12/27/2023,12/28/2023,12/29/2023,12/30/2023,01/01/2024,01/02/2024,01/03/2024,01/04/2024,01/05/2024,01/06/2024,01/08/2024,01/09/2024,01/10/2024,01/11/2024,01/12/2024,01/13/2024,01/15/2024,01/16/2024,01/17/2024,01/20/2024,01/28/2024,01/31/2024,02/02/2024,02/18/2024,02/19/2024,02/22/2024,02/23/2024,03/01/2024,03/02/2024,03/03/2024,03/05/2024,03/06/2024,03/07/2024,01/25/2024,01/26/2024,03/08/2024,01/27/2024,01/29/2024,02/01/2024,02/03/2024,08/03/2023,02/04/2024,03/09/2024,03/10/2024 12/12/2023,12/13/2023,12/14/2023,12/15/2023,12/16/2023,12/17/2023,12/19/2023,12/20/2023,12/21/2023,12/22/2023 12/17/2023, 12/19/2023 10/22/2023, 3/9/2024 10/14/2023,12/13/2023,12/21/2023 12/12/2023, 12/13/2023 12/28/2023,12/29/2023,01/01/2024,01/03/2024,01/08/2024,01/10/2024,01/11/2024,01/12/2024 10/15/2023 1/11/2024 2/10/2024
- Quantity
- 959,387 units (total)
Why it was recalled
Foreign material in product. Pieces of cleaning brush bristles found in the product
Recalling firm
- Firm
- Sanders Candy LLC dba Second Nature Brands
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 23770 Hall Rd, Clinton Township, Michigan 48036-1275
Distribution
- Distribution pattern
- Nationwide and Canada
Timeline
- Recall initiated
- 2022-12-22
- FDA classified
- 2023-01-10
- Posted by FDA
- 2023-01-18
- Terminated
- 2024-08-05
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0248-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings.