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CriticalFDAfda-F-1795-2015UNDECLARED ALLERGEN

Cumin Ground, 2.75 oz., UPC: 811267012008. Product is packaged in a plastic bottle with a black flip-top lid.

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
99
Recall Date
January 28, 2015
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1795-2015.

Product may contain undeclared peanut protein.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1795-2015.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact The Spicemill Llc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1795-2015.

The Spicemill LLC.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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The Spicemill Llc. Recall FAQ

The Spicemill Llc. is the subject of a food safety report: Cumin Ground, 2.75 oz., UPC: 811267012008. Product is packaged in a plastic bottle with a black flip-top lid.. The notice was published on January 28, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 99 units are potentially affected.