MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB.
Recalling firm: Morton Salt Inc.
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 20, 2020.
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FDA code information
Lot #SS19275025; UPC: 2460001001; Best By: 9/30/2024
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Full FDA record and distribution details
Original product description
MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| best by | 9/30/2024 | Lot #SS19275025; UPC: 2460001001; Best By: 9/30/2024 |
| lot | SS19275025 | Lot #SS19275025; UPC: 2460001001; Best By: 9/30/2024 |
Original FDA recall reason
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.
Recall details
- Recall number
- F-0682-2020
- Event ID
- 84767
- FDA status
- Terminated
- Initiated
- Jan 22, 2020
- Reported
- Feb 19, 2020
- Classified
- Feb 11, 2020
- Terminated
- Feb 20, 2020
- Quantity
- 4 pallets at 1344 canisters per pallet (5,376 canisters)
- Location
- Silver Springs, NY, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
NC
Data updated September 16, 2026. View official FDA data ↗
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