Check the Batch
Class IIITerminated in FDA datasetRecall initiated Jun 2, 2025

Windsor brand Extra Course Sea Salt Grinder Refill, 255 g, packaged in a glass jar with plastic…

Recalling firm: MORTON SALT INC

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 28, 2026.

Check your package

Compare the exact product and package details with the label you have.

ProductWindsor 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
Package size255 g

FDA code information

UPC: 6601007997; Case UPC: 10066010079976; Batch: ZI25034001, ZI25035001, ZI25036001, ZI25037001

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original 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

Extracted codes and context

TypeCode / valueContext
batchZI25034001UPC: 6601007997; Case UPC: 10066010079976; Batch: ZI25034001, ZI25035001, ZI25036001, ZI25037001
batchZI25035001UPC: 6601007997; Case UPC: 10066010079976; Batch: ZI25034001, ZI25035001, ZI25036001, ZI25037001
batchZI25036001UPC: 6601007997; Case UPC: 10066010079976; Batch: ZI25034001, ZI25035001, ZI25036001, ZI25037001
batchZI25037001601007997; Case UPC: 10066010079976; Batch: ZI25034001, ZI25035001, ZI25036001, ZI25037001

Original FDA recall reason

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

Recall details

Recall number
H-0062-2025
Event ID
97013
FDA status
Terminated
Initiated
Jun 2, 2025
Reported
Jul 2, 2025
Classified
Jun 20, 2025
Terminated
Apr 28, 2026
Quantity
28,820 units
Location
Chicago, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

All product exported for sale in Canada only.

FDA source record · H-0062-2025

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.