Private Selection Chocolate Hazelnut Mascarpone Ice Cream, 16 fl oz lamented carton. Product labeled in part, "PRIVATE SELECTION" CHOCOLATE HAZELNUT MASCARPONE ICE CREAM chocolate covered hazelnuts folded into creamy mascarpone ice cream***INGREDIENTS: ICE CREAM MILK, CREAM SUGAR***MASCARPONE CHEESE (MILK, CREAM, CITRIC ACID)***CONTAINS: MILK, SOY, HAZELNUT***DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 UPC: 0 11110 52101 9

Class I - Dangerous
Recalled: April 25, 2014 Kroger Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    ALL CODES
  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:
Kroger Co
Reason for Recall:
The firm discovered that the label for two of their products did not declare eggs in the ingredient statement.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Private Selection Chocolate Hazelnut Mascarpone Ice Cream, 16 fl oz lamented carton. Product labeled in part, "PRIVATE SELECTION" CHOCOLATE HAZELNUT MASCARPONE ICE CREAM chocolate covered hazelnuts folded into creamy mascarpone ice cream***INGREDIENTS: ICE CREAM MILK, CREAM SUGAR***MASCARPONE CHEESE (MILK, CREAM, CITRIC ACID)***CONTAINS: MILK, SOY, HAZELNUT***DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 UPC: 0 11110 52101 9

Product Codes/Lot Numbers:

ALL CODES

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1941-2014

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