F-0682-2020 Class III Terminated

Recalled by Morton Salt Inc. — Silver Springs, NY

FDA food recall F-0682-2020 was initiated by Morton Salt Inc. on Jan 22, 2020 and is designated Class III. Reason for recall: Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients. The recall status is terminated (terminated Feb 20, 2020). Affected quantity: 4 pallets at 1344 canisters per pallet (5,376 canisters).

Recall Details

Product Type
Food
Report Date
Feb 19, 2020
Initiation Date
Jan 22, 2020
Termination Date
Feb 20, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4 pallets at 1344 canisters per pallet (5,376 canisters)

Product Description

MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case

Reason for Recall

Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.

Distribution Pattern

NC

Code Information

Lot #SS19275025; UPC: 2460001001; Best By: 9/30/2024

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0682-2020
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for F-0682-2020. Report a data issue: hello@regdatalab.com.