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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 84767

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
January 22, 2020
Product types
Food
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Morton Salt Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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

F-0682-2020
Recall number
F-0682-2020
Initiated
January 22, 2020
Classification
Class III
Status
Terminated
Recalling firm
Morton Salt Inc.
Quantity
4 pallets at 1344 canisters per pallet (5,376 canisters)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

NC