Chili Powder, Mild, Organic is a blend, Item # 90030. Packaged in 1 lb. bags and sold under brand Azure Market. This product contains "Organic Chili Peppers, Salt, Organic Spices, Organic Garlic, Organic Sunflower Oil". The Azure Market label listed the lot # 90030041520 and UPC 8 70722 00251 0.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Azure Market label listed the lot # 90030041520. KFK Lot # 041520. The KFK's 6-digit lot coding is generally the date the order was submitted and input into KFK's system and may not align with actual production date.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- K F K Seasonings Llc
- Reason for Recall:
- Undeclared tree nuts and Crustacea.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Chili Powder, Mild, Organic is a blend, Item # 90030. Packaged in 1 lb. bags and sold under brand Azure Market. This product contains "Organic Chili Peppers, Salt, Organic Spices, Organic Garlic, Organic Sunflower Oil". The Azure Market label listed the lot # 90030041520 and UPC 8 70722 00251 0.
Product Codes/Lot Numbers:
Azure Market label listed the lot # 90030041520. KFK Lot # 041520. The KFK's 6-digit lot coding is generally the date the order was submitted and input into KFK's system and may not align with actual production date.
Distribution:
Distributed in: OR, UT
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0972-2020
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