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Class III: unlikely to cause harmTerminated

Morton Recall

Morton, Sodium Chloride, USP, Granular, packaged in kraft paper bags, fiber drums, and…

Morton Salt Co. · Chicago, IL

Risk level
Class III
Reported by FDA
Aug 29, 2012
Recall ID
D-1656-2012
Check your lot numberHow we source this data

Summary

Morton Salt recalled Morton starting May 8, 2012. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1656-2012 on Aug 29, 2012. Reason: Impurities/Degradation Products: The product was found to contain a slightly out of specification level of bromides, exceeding the bromides limit for USP Sodium Chloride. Status: Terminated.

Why it was recalled

Impurities/Degradation Products: The product was found to contain a slightly out of specification level of bromides, exceeding the bromides limit for USP Sodium Chloride.

Product description

Morton, Sodium Chloride, USP, Granular, packaged in kraft paper bags, fiber drums, and semi-bulk bags. Product is shipped in 80 lb bags, 350 lb drums & 2000 lb semi-bulk sacks. Manufactured by Morton Salt, Inc., Chicago, Illinois 60606-1743.

Lot numbers, UPCs & expiration codes

Lot #: OCT251BC01, NOV041BA01 & NOV071BA01.

Where it was sold

Nationwide & PR & Ireland.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1656-2012
Classification
Class III
Status
Terminated
Recall initiated
May 8, 2012
FDA report date
Aug 29, 2012
Quantity
531,950 lbs
Recall type
Voluntary: Firm initiated
Recalling firm
Morton Salt Co.

Original FDA data

Every field from FDA enforcement report D-1656-2012, exactly as published.

Show all FDA fields
City
Chicago
State
IL
Status
Terminated
Country
United States
Event ID
61818
Address
123 N Wacker Dr
Code information
Lot #: OCT251BC01, NOV041BA01 & NOV071BA01.
Postal code
60606-1743
Report date
Aug 29, 2012
Product type
Drugs
Recall number
D-1656-2012
Classification
Class III
Recalling firm
Morton Salt Co.
Product quantity
531,950 lbs
Termination date
Mar 1, 2013
Reason for recall
Impurities/Degradation Products: The product was found to contain a slightly out of specification level of bromides, exceeding the bromides limit for USP Sodium Chloride.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Morton, Sodium Chloride, USP, Granular, packaged in kraft paper bags, fiber drums, and semi-bulk bags. Product is shipped in 80 lb bags, 350 lb drums & 2000 lb semi-bulk sacks. Manufactured by Morton Salt, Inc., Chicago, Illinois 60606-1743.
Distribution pattern
Nationwide & PR & Ireland.
Recall initiation date
May 8, 2012
Initial firm notification
Letter
Center classification date
Aug 20, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1656-2012, published Aug 29, 2012. 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. Medication information here is not individualized medical advice.

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