United Salt Corp Recalls Salt Due to Mislabeling
United Salt Corp is recalling salt because plain salt was labeled as iodized and iodized salt was labeled as plain, a mislabeling issue.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: This is an FDA Class III recall, which by definition is not reasonably likely to cause adverse health consequences. No illnesses or injuries have been reported, and the hazard is limited to mislabeling.
Plain-English summary
United Salt Corp is recalling salt due to mislabeling. Plain salt was incorrectly labeled as iodized, and iodized salt was incorrectly labeled as plain.
The recall affects 10,160 cans of salt distributed in Texas. The code information is listed as tba.
This is a Class III recall, meaning it is not reasonably likely to cause adverse health consequences. No illnesses or injuries have been reported in connection with this recall.
Consumers who have the recalled salt should not eat it if they have a medical condition that requires avoiding iodine or avoiding added iodine. They should contact United Salt Corp for a replacement or refund.
The recalled product
- Product
- Salt
- Manufacturer
- United Salt Corp
- Category
- Food — Salt
- Hazard
- Affected units
- 10,160
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- tba
Distribution
Distributed in 1 state:
Related recalls
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02