FDA recall record

MORTON SALT Windsor brand Extra Course Sea Salt Grinder Refill, 255 g recall — FDA H-0062-2025

The quantity of product in each unit does not match the stated weight.

Class IIIclassification
H-0062-2025official record ID
Jul 2, 2025report date

Recall record at a glance

Official recordH-0062-2025
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmMORTON SALT Inc.
Report dateJul 2, 2025
Recall initiation dateJun 2, 2025
Quantity28,820 units
LocationChicago, IL, United States

Official product description

Windsor brand Extra Course Sea Salt Grinder Refill, 255 g, packaged in a glass jar with plastic lid and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9

Why the product was recalled

The quantity of product in each unit does not match the stated weight.

Distribution information

All product exported for sale in Canada only.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.