How many FDA recalls has MORTON SALT INC had?

The FDA has published 6 food recall enforcement records naming MORTON SALT INC between 2018 and 2025. Those records cover 5 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.

Does a high recall count mean a firm is unsafe?

Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

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MORTON SALT INC FDA recall records

The FDA has published 6 food recall enforcement records naming MORTON SALT INC between 2018 and 2025, covering 5 separate recall events. The firm is recorded in Illinois. Data last updated 2 September 2026.

Records of 29,386: 6
Share of all recalls: 0%
Class I of 6: 0
Reported between: 2018 to 2025

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 6 records cover 5 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

0 of these records are Class I, 0 Class II and 6 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

What was recalled for

A single record can name more than one hazard, so these counts overlap.

Undeclared allergens1

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Year	Recalls reported
2012	0
2013	0
2014	0
2015	0
2016	0
2017	0
2018	1
2019	0
2020	1
2021	1
2022	0
2023	0
2024	1
2025	2
2026	0

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 6 records.
Reported	Product	Firm	Reason	Class
2025-07-02	Windsor brand Extra Course Sea Salt Grinder Refill, 255 g, packaged in a glass jar with plastic lid and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9	MORTON SALT INC	The quantity of product in each unit does not match the stated weight.	Class III
2025-07-02	Windsor brand Extra Course Himalayan Pink Salt Grinder Refill, 255 g, packaged in a glass jar with plastic cap and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9	MORTON SALT INC	The quantity of product in each unit does not match the stated weight.	Class III
2024-04-24	Windsor Black Peppercorns, 34g grinder, UPC 0 66010 08200 9, 6 units per wholesale case	MORTON SALT INC	Label mix-up product is labeled as black peppercorn but is actually Pink Himalayan salt	Class III
2021-12-22	Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago, IL 60606	MORTON SALT INC	Product labeled to contain iodized salt actually contain salt not fortified with iodine.	Class III
2020-02-19	MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case	Morton Salt Inc.	Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.	Class III
2018-09-05	MORTON NATURAL SEA SALT ALL PURPOSE*NET WET 26 OZ (1 LB 10 OZ) 737 gNutrition FactsINGREDIENTS: SEA SALT PRODUCT OF BAHAMASMORTON SALE, INC, CHICAGO, IL 60606**QUESTIONS? CALL 1-800-789-SALT (7258)	MORTON SALT INC	Iodized sea salt was packaged in Morton Natural Sea Salt packages.	Class III

Questions

How many FDA recalls has MORTON SALT INC had?: The FDA has published 6 food recall enforcement records naming MORTON SALT INC between 2018 and 2025. Those records cover 5 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?: Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.