RecallHawk
Class III Recall

Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago, IL 60606

MORTON SALT INC

Summary

The FDA issued a Class III for Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago by MORTON SALT INC. Reason: Product labeled to contain iodized salt actually contain salt not fortified with iodine..

Details

Source

Food Recall

External ID

F-0334-2022

Action Date

2021-12-22

Status

Terminated

Category

food

Product Description

Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago, IL 60606

Lot/Code Info: Best By 9/8/2026

Quantity Affected: 16,920 canisters

Reason for Recall

Product labeled to contain iodized salt actually contain salt not fortified with iodine.

Distribution

Distributed to retailers in Colorado and California

Type: Voluntary: Firm initiated

Recall Initiated: 2021-12-01

Company

MORTON SALT INC

Chicago, IL

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.

MORTON SALT INC has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MORTON SALT INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does MORTON SALT INC have FDA actions?

MORTON SALT INC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0334-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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