Windsor brand Extra Course Himalayan Pink Salt Grinder Refill, 255 g, packaged in a…
MORTON SALT INC recalled this product and the FDA reported the enforcement action on 2 July 2025 as Class III. The recall was initiated by the firm. The quantity of product in each unit does not match the stated weight.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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
- Reason for recall
- The quantity of product in each unit does not match the stated weight.
- Recalling firm
- MORTON SALT INC
- Firm location
- Chicago, Illinois, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- H-0061-2025
- Quantity
- 36,882 units
- Distribution
- All product exported for sale in Canada only.
- Initiated
- 2 June 2025
- Reported by FDA
- 2 July 2025
- Terminated
- 28 April 2026
- Firm notified by
- Product codes
- UPC: 6601007998; Case UPC: 10066010079983; Batch: ZI25056008, ZI25057001, ZI25058001, ZI25106001, ZI25107001
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
- The recall ran for 11 months, from 2 June 2025 to termination on 28 April 2026. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The FDA published the enforcement report 4 weeks after the firm began the recall.
- Recalls of a spice or seasoning run a median of 6 months, so this one was longer than usual for its category. Spices are a low-moisture, globally sourced, minimally processed ingredient that is added after any kill step, which is the combination that makes Salmonella in a spice lot capable of contaminating every product it was blended into.
Filed under spices and seasonings. A product can sit in more than one.
Every product in this recall
The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-07-02 | 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 | MORTON SALT INC | The quantity of product in each unit does not match the stated weight. | Class III |
Other spices and seasonings recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from MORTON SALT INC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 5 other records name this firm.
All 6 records for MORTON SALT INC
All 2025 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.