deLISH, fresh, Pineapple, mango, & cantaloupe spears ( 5 oz), UPC 0.49022-53701.9 and tropical medley, (10 oz), UPC 0.49022-53699.9. Prepared for Walgreen, Inc. Deerfield, IL 60015. Ingredients: Cantaloupe, Mango, Pineapple, Packed in its Own Juice, Grown In USA, Mexico, Costa Rica

Class I - Dangerous
🍎 Food Recalled: September 15, 2012 Caito Foods Service Produce Nationwide

What Should You Do?

  1. Check if you have this product:
    Spears:Item 383138; Best By 8/04/12 -09/14/12 Medey :item 383137; Best By 8/04/12 -09/14/12
  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:
Caito Foods Service, Inc.
Reason for Recall:
In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

deLISH, fresh, Pineapple, mango, & cantaloupe spears ( 5 oz), UPC 0.49022-53701.9 and tropical medley, (10 oz), UPC 0.49022-53699.9. Prepared for Walgreen, Inc. Deerfield, IL 60015. Ingredients: Cantaloupe, Mango, Pineapple, Packed in its Own Juice, Grown In USA, Mexico, Costa Rica

Product Codes/Lot Numbers:

Spears:Item 383138; Best By 8/04/12 -09/14/12 Medey :item 383137; Best By 8/04/12 -09/14/12

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0128-2013

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