F-1909-2018 Class III Terminated

Recalled by MORTON SALT INC — Chicago, IL

FDA food recall F-1909-2018 was initiated by MORTON SALT INC on Aug 9, 2018 and is designated Class III. Reason for recall: Iodized sea salt was packaged in Morton Natural Sea Salt packages. The recall status is terminated (terminated Mar 8, 2019). Affected quantity: 22,284 Units (1857 cases).

Recall Details

Product Type
Food
Report Date
Sep 5, 2018
Initiation Date
Aug 9, 2018
Termination Date
Mar 8, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
22,284 Units (1857 cases)

Product Description

MORTON NATURAL SEA SALT ALL PURPOSE***NET WET 26 OZ (1 LB 10 OZ) 737 g***Nutrition Facts***INGREDIENTS: SEA SALT PRODUCT OF BAHAMAS***MORTON SALE, INC, CHICAGO, IL 60606***QUESTIONS? CALL 1-800-789-SALT (7258)

Reason for Recall

Iodized sea salt was packaged in Morton Natural Sea Salt packages.

Distribution Pattern

Products were distributed in the following states: FL, MD, ME, MI, NH, NJ, NY, PA, and VA.

Code Information

RI18162021

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-1909-2018
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-1909-2018. Report a data issue: hello@regdatalab.com.