Windsor brand Extra Course Himalayan Pink Salt Grinder Refill, 255 g, packaged in a glass jar with plastic cap and packe
Summary
The FDA issued a Class III for Windsor brand Extra Course Himalayan Pink Salt Grinder Refill, 255 g, packaged i by MORTON SALT INC. Reason: The quantity of product in each unit does not match the stated weight..
Details
Source
Food Recall
External ID
H-0061-2025
Action Date
2025-07-02
Status
Terminated
Category
food
Product Description
Windsor brand Extra Course Himalayan Pink Salt Grinder Refill, 255 g, packaged in a glass jar with plastic cap and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9
Lot/Code Info: UPC: 6601007998; Case UPC: 10066010079983; Batch: ZI25056008, ZI25057001, ZI25058001, ZI25106001, ZI25107001
Quantity Affected: 36,882 units
Reason for Recall
The quantity of product in each unit does not match the stated weight.
Distribution
All product exported for sale in Canada only.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-02
Company
Chicago, IL
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
MORTON SALT INC has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MORTON SALT INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MORTON SALT INC have FDA actions?
MORTON SALT INC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0061-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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