Yellow rice mixes with the following g brand names: (1) Shurfine brand Yellow Rice with Saffron, NET WT 5 OZ (142g), distributed by TOPCO ASSOCIATES, LLC, 7711 GROSS POINT ROAD, SKOKIE, IL 60077. UPC 011161159834 and (2) Hannaford brand Yellow Rice with real saffron & other seasonings, NET WT. 5 OZ (142g), distributed by HANNAFORD BROS. CO., SCARBOROUGH, ME 04074. UPC 041268184699

Class I - Dangerous
Recalled: December 7, 2012 Riviana International Other Foods

What Should You Do?

  1. Check if you have this product:
    Shurfine: BEST BY: March 2013, 259M120 Hannaford: BEST BY MARCH 2014, 250M219
  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:
Riviana International, Inc
Reason for Recall:
Undeclared hydrolyzed soy protein in yellow rice with saffron
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Yellow rice mixes with the following g brand names: (1) Shurfine brand Yellow Rice with Saffron, NET WT 5 OZ (142g), distributed by TOPCO ASSOCIATES, LLC, 7711 GROSS POINT ROAD, SKOKIE, IL 60077. UPC 011161159834 and (2) Hannaford brand Yellow Rice with real saffron & other seasonings, NET WT. 5 OZ (142g), distributed by HANNAFORD BROS. CO., SCARBOROUGH, ME 04074. UPC 041268184699

Product Codes/Lot Numbers:

Shurfine: BEST BY: March 2013, 259M120 Hannaford: BEST BY MARCH 2014, 250M219

Distribution:

Distributed in: FL, WI, ME, NY

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0851-2013

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