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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Packaged & Processed

Windsor Black Peppercorns Recalled for Label Mix-up with Himalayan Salt

Agency Publication Date: April 12, 2024
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Summary

Morton Salt Inc. has recalled approximately 1,423 cases of Windsor Black Peppercorns (34g grinder) because the product was mislabeled. The grinders actually contain Pink Himalayan salt instead of black peppercorns. No incidents or injuries have been reported to date. Consumers who purchased the affected product should return it to the place of purchase for a refund or dispose of it.

Risk

The product is mislabeled and contains Pink Himalayan salt instead of black peppercorns. While the risk is low, consumers will be using salt when they intended to use pepper, which may impact individuals monitoring their sodium intake.

What You Should Do

  1. This recall affects Windsor Black Peppercorns sold in 34g grinders with UPC 066010082009 and lot code ZX23060001.
  2. Check the back of the grinder packaging to identify the 12-digit UPC 066010082009 and the lot code ZX23060001.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Windsor Black Peppercorns (34g grinder)
UPC Codes:
066010082009
Lot Numbers:
ZX23060001

6 units per wholesale case; Recall #: F-1149-2024

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94344
Status: Resolved
Manufacturer: MORTON SALT INC
Manufactured In: United States
Units Affected: 1423 cases

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.