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

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

Recall #: F-0334-2022
Affected scope: 16,920 canisters
Initiated: December 1, 2021

Compiled from official public sources by the publisher. · Updated September 2026

Morton Salt INC recalled Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago, IL 60606 - a low-severity action.

Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago, IL 60606 was recalled by Morton Salt INC in December 22, 2021. Reason: Product labeled to contain iodized salt actually contain salt not fortified with iodine.. Check the official notice for the remedy. Verify recall #F-0334-2022 with the FDA Food before acting.

The recall

Morton Salt INC issued this low-severity FDA Food recall-Product labeled to contain iodized salt actually contain salt not fortified with iodine..

Low
severity level: Class III
classification: December 22, 2021
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0334-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

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

Reason for recall

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

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Low (Class III)
Status	Terminated
Recall number	F-0334-2022
Date reported	December 22, 2021
Date initiated	December 1, 2021
Recalling firm	Morton Salt INC
Firm location	Chicago, IL
Affected scope	16,920 canisters
Distribution	Distributed to retailers in Colorado and California

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-0334-2022) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago, IL 60606. Recalled by Morton Salt INC. Units affected: 16,920 canisters.

Why was this product recalled? ▼

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

Which agency issued this recall? ▼

This recall was issued by the FDA Food on December 22, 2021. Severity: Low. Recall number: F-0334-2022.

Where was the recalled product distributed? ▼

Distribution: Distributed to retailers in Colorado and California.

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Low), closest by report date among other firms and states.

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Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported December 22, 2021. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026