FindMyRecallSubscribe
Class III: unlikely to cause harmTerminated

Morton Salt Recall

MORTON SALT

Morton Salt Inc. · Silver Springs, NY

Risk level
Class III
Reported by FDA
Feb 19, 2020
Recall ID
F-0682-2020
Check your lot numberHow we source this data

Summary

Morton Salt recalled Morton Salt starting Jan 22, 2020. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-0682-2020 on Feb 19, 2020. Reason: Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients. Status: Terminated.

Why it was recalled

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

Product description

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

Lot numbers, UPCs & expiration codes

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

Where it was sold

NC

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-0682-2020
Classification
Class III
Status
Terminated
Recall initiated
Jan 22, 2020
FDA report date
Feb 19, 2020
Quantity
4 pallets at 1344 canisters per pallet (5,376 canisters)
Recall type
Voluntary: Firm initiated
Recalling firm
Morton Salt Inc.

Original FDA data

Every field from FDA enforcement report F-0682-2020, exactly as published.

Show all FDA fields
City
Silver Springs
State
NY
Status
Terminated
Country
United States
Event ID
84767
Address
45 Ribaud Ave
Code information
Lot #SS19275025; UPC: 2460001001; Best By: 9/30/2024
Postal code
14550-9805
Report date
Feb 19, 2020
Product type
Food
Recall number
F-0682-2020
Classification
Class III
Recalling firm
Morton Salt Inc.
Product quantity
4 pallets at 1344 canisters per pallet (5,376 canisters)
Termination date
Feb 20, 2020
Reason for recall
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.
Voluntary / mandated
Voluntary: Firm initiated
Product description
MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case
Distribution pattern
NC
Recall initiation date
Jan 22, 2020
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Feb 11, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0682-2020, published Feb 19, 2020. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls