FDA recall record
MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of February 20, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case
Reason
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case
Code information listed by FDA
Lot #SS19275025; UPC: 2460001001; Best By: 9/30/2024
Distribution and firm information
Recalling firm listed by FDA: Morton Salt Inc.
Firm location listed by FDA: Silver Springs, NY, United States
Distribution reported by FDA: NC
Product quantity listed by FDA: 4 pallets at 1344 canisters per pallet (5,376 canisters)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.