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Class III: unlikely to cause harmTerminated

Morton Natural Sea Salt All Purpose***Net Recall

MORTON NATURAL SEA SALT ALL PURPOSE***NET WET 26 OZ (1 LB 10 OZ) 737 g***Nutrition Fact…

MORTON SALT INC · Chicago, IL

Risk level
Class III
Reported by FDA
Sep 5, 2018
Recall ID
F-1909-2018
Check your lot numberHow we source this data

Summary

Morton Salt recalled Morton Natural Sea Salt All Purpose***Net starting Aug 9, 2018. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1909-2018 on Sep 5, 2018. Reason: Iodized sea salt was packaged in Morton Natural Sea Salt packages. Status: Terminated.

Why it was recalled

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

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)

Lot numbers, UPCs & expiration codes

RI18162021

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1909-2018
Classification
Class III
Status
Terminated
Recall initiated
Aug 9, 2018
FDA report date
Sep 5, 2018
Quantity
22,284 Units (1857 cases)
Recall type
Voluntary: Firm initiated
Recalling firm
MORTON SALT INC

Original FDA data

Every field from FDA enforcement report F-1909-2018, exactly as published.

Show all FDA fields
City
Chicago
State
IL
Status
Terminated
Country
United States
Event ID
80848
Address
444 W Lake St #3000
Code information
RI18162021
Postal code
60606
Report date
Sep 5, 2018
Product type
Food
Recall number
F-1909-2018
Classification
Class III
Recalling firm
MORTON SALT INC
Product quantity
22,284 Units (1857 cases)
Termination date
Mar 8, 2019
Reason for recall
Iodized sea salt was packaged in Morton Natural Sea Salt packages.
Voluntary / mandated
Voluntary: Firm initiated
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)
Distribution pattern
Products were distributed in the following states: FL, MD, ME, MI, NH, NJ, NY, PA, and VA.
Recall initiation date
Aug 9, 2018
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Mar 7, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1909-2018, published Sep 5, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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