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Lower risk Food recall · FDA · Published June 2, 2025

Morton Windsor Sea Salt Refills: Incorrect Weight in Glass Jars

Morton recalls Windsor brand Extra Course Sea Salt Grinder Refills (255g) due to weight discrepancy. Check UPC 6601007997 for affected units. No action needed if weight is within tolerance.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-0062-2025FoodMorton ›
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Recalling firmMORTON SALT INC444 W Lake St #3000 · Chicago, IL 60606
✎ GovInfoNow plain-language explainer

Morton is recalling Windsor brand Extra Course Sea Salt Grinder Refills that weigh less than advertised. This means you might be getting less salt than expected, but it doesn't pose a safety risk. Read more at govinfonow.com/recall/7758-morton-windsor-sea-salt-refills-incorrect-weight-in-glass-jars.

Source Summary by GovInfoNow · govinfonow.com/recall/7758-morton-windsor-sea-salt-refills-incorrect-weight-in-glass-jars · Updated August 17, 2026 · Official notice: FDA #H-0062-2025

Cite this page

“Morton Windsor Sea Salt Refills: Incorrect Weight in Glass Jars.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/7758-morton-windsor-sea-salt-refills-incorrect-weight-in-glass-jars. Based on FDA recall #H-0062-2025.

The FDA announced on June 2, 2025, that Morton Salt Inc. is recalling Windsor brand Extra Course Sea Salt Grinder Refill because the quantity in each unit does not match the stated weight. The agency issued recall number H-0062-2025 for the Class III voluntary recall.

How to tell if you have it

  • Brand: Windsor
  • Product: Extra Course Sea Salt Grinder Refill, 255 g, packaged in a glass jar with plastic lid and packed 6 units
  • UPC: 6601007997
  • Case UPC: 10066010079976
  • Batch codes: ZI25034001, ZI25035001, ZI25036001, ZI25037001

The hazard

According to the FDA, the hazard is that the quantity of product in each unit does not match the stated weight. The record provides no information regarding incidents or injuries.

Context

GovInfoNow's records show MORTON SALT INC has 4 other recalls on record since 2018-08-09. Other recent recalls of similar products include Morton Salt Recalls Windsor Black Peppercorn Grinder Due to Label Error (2024-03-29), Morton Iodized Salt Lacks Iodine - Recall for Non-Iodized Salt (2021-12-01), and Morton Salt Recall: Iodide Missing in 26oz Salt Canisters (2020-01-22). Spicely Organic Sumac Recall: Salt Mislabeling Hazard occurred on 2026-01-14.

How to tell if you have this one

Check for the UPC 6601007997 on the product packaging. The product comes in glass jars with plastic lids, packaged 6 units per case. The batch numbers ZI25034001 through ZI25037001 are also on the packaging.

  • Brand
    Morton
  • Product
    Windsor brand Extra Course Sea Salt Grinder Refill, 255 g, packaged in a glass jar with plastic lid and packed 6 units
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class III
  • Status
    Terminated
  • Distribution
    All product exported for sale in Canada only.
Recall numberProduct, codes & lotsQuantity
H-0061-2025Windsor 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; UPC: 6601007998; Case UPC: 10066010079983; Batch: ZI25056008, ZI25057001, ZI25058001, ZI25106001, ZI2510700136,882 units
H-0062-2025Windsor 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; UPC: 6601007997; Case UPC: 10066010079976; Batch: ZI25034001, ZI25035001, ZI25036001, ZI2503700128,820 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Weight

    Verify the weight on the product label matches the advertised 255 grams. If it's less, the product may be affected.

How this recall unfolded

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Jun 2, 202512. FDA classified it Class III: Jun 20, 202523. Published in FDA’s Enforcement Report: Jul 2, 202534. FDA terminated the recall: Apr 28, 2026420252026
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0062-2025 (June 2, 2025)
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA