Masas Gourmet Curry Coconut Sauce, packaged in a glass jar with gold metal cap, net wt. 12 oz. (355 mL), UPC 786764412227.

Class I - Dangerous
Recalled: June 16, 2017 Rikki USA Other Foods

What Should You Do?

  1. Check if you have this product:
    Lot # 1740138 Best by Date: 10/6/2018. Lot # 1740099 Best by Date: 9/9/2018. Lot # 1740065 Best by Date: 8/23/2018. Lot # 1640480 Best by Date: 4/28/2018. Lot # 1640416 Best by Date: 3/19/2018. Lot # 1640311 Best by Date: 1/11/2018. Lot # 1640197 Best by Date: 11/9/2017. Lot # 1640056 Best by Date: 8/16/2017.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Rikki USA, Inc.
Reason for Recall:
Curry Coconut Sauce is recalled because the Ingredients Statement declared dry whey but the Contains statement does not declare milk.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Masas Gourmet Curry Coconut Sauce, packaged in a glass jar with gold metal cap, net wt. 12 oz. (355 mL), UPC 786764412227.

Product Codes/Lot Numbers:

Lot # 1740138 Best by Date: 10/6/2018. Lot # 1740099 Best by Date: 9/9/2018. Lot # 1740065 Best by Date: 8/23/2018. Lot # 1640480 Best by Date: 4/28/2018. Lot # 1640416 Best by Date: 3/19/2018. Lot # 1640311 Best by Date: 1/11/2018. Lot # 1640197 Best by Date: 11/9/2017. Lot # 1640056 Best by Date: 8/16/2017.

Distribution:

Distributed in: CA, IL, NY, OR, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2586-2017

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