CLASS III Food recall · Reported 19 Feb 2020 · FDA Enforcement Report
This Salt Does Not Supply Iodide recalled by Morton Salt
Morton Salt is recalling Morton Salt;this Salt Does Not Supply Iodide, distributed in North Carolina. The recall was initiated on 22 Jan 2020 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0682-2020
- FDA event ID
- 84767
- Recalling firm
- Morton Salt, Silver Springs, NY
- Brand
- Morton Salt
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 22 Jan 2020
- FDA classified
- 11 Feb 2020
- Reported
- 19 Feb 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Allergens
- Product category
- Other
Timeline
| 22 Jan 2020 | Recall initiated by company | |
| 11 Feb 2020 | Classified by FDA | +20 days |
| 19 Feb 2020 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case
Where it was distributed
NC
Questions about this recall
Is This Salt Does Not Supply Iodide recalled?
Yes. Morton Salt recalled This Salt Does Not Supply Iodide on 22 Jan 2020. The recall is Class III and its status is Terminated. Recall number F-0682-2020.
Why was it recalled?
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.
Which lots are affected?
Lot #SS19275025; UPC: 2460001001; Best By: 9/30/2024
Where was it sold?
NC
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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