🔍 RecallPedia

Italian blend Salad (Romaine Lettuce and Radicchio) packaged under the following brand names: Dole Italian Blend, (UPC 7143000819); Fresh Selections Italian Style Blend (Kroger) (UPC 1111091045); Little Salad Bar Italian Salad, (UPC 4149811014); Marketside Italian Style Salad, (Wal Mart) (UPC 8113102780) 10 oz. bags (283 g) Dole Fresh Vegetables Monterey, CA 93942

Class I - Dangerous
Recalled: March 13, 2014 Dole Fresh Vegetables Produce

What Should You Do?

  1. Check if you have this product:
    A058201A, A058201B, Best By March 12, 2014.
  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:
Dole Fresh Vegetables Inc
Reason for Recall:
Canadian Food Inspection Agency tested a random sample of bagged Italian Blend which tested positive for Listeria Monocytogenes.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Italian blend Salad (Romaine Lettuce and Radicchio) packaged under the following brand names: Dole Italian Blend, (UPC 7143000819); Fresh Selections Italian Style Blend (Kroger) (UPC 1111091045); Little Salad Bar Italian Salad, (UPC 4149811014); Marketside Italian Style Salad, (Wal Mart) (UPC 8113102780) 10 oz. bags (283 g) Dole Fresh Vegetables Monterey, CA 93942

Product Codes/Lot Numbers:

A058201A, A058201B, Best By March 12, 2014.

Distribution:

Distributed in: CT, FL, IL, IN, KY, MA, MD, MI, NC, NJ, NY, OH, PA, SC, VA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1702-2014

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