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Mixed Fruit Products that contain Cantaloupe, Honeydew, Pineapple, and Red Grapes Identified with the following Item ID and Description. 1. 11658 Fruit Mix, CHPG 5lb. (GR#11658) 2. 4703 Fruit Spear CHWP 15oz 3. 4768 Fruit Mix CHPG 6.5oz Lacer 4. 4774 Fruit Mix, CrGHP 6-6.5oz Lacer 5. 4852 Fruit Tray Round 2.5lb. 6. 9038716 Fruit Mix CrgHP 24-6oz Lacert 7. ET612 Fruit Mix CHPG 6/16 oz.

Class I - Dangerous
Recalled: November 24, 2023 Cut Fruit Express Produce

What Should You Do?

  1. Check if you have this product:
    1. 11/5/23 2. 11/5/23 3. 11/4/23 4. 11/4/23 5. 11/5/23 6. 11/3/23 and 11/4/23 7. 11/5/23
  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:
Cut Fruit Express, Inc.
Reason for Recall:
Cantaloupe containing products may be contaminated with Salmonella.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Mixed Fruit Products that contain Cantaloupe, Honeydew, Pineapple, and Red Grapes Identified with the following Item ID and Description. 1. 11658 Fruit Mix, CHPG 5lb. (GR#11658) 2. 4703 Fruit Spear CHWP 15oz 3. 4768 Fruit Mix CHPG 6.5oz Lacer 4. 4774 Fruit Mix, CrGHP 6-6.5oz Lacer 5. 4852 Fruit Tray Round 2.5lb. 6. 9038716 Fruit Mix CrgHP 24-6oz Lacert 7. ET612 Fruit Mix CHPG 6/16 oz.

Product Codes/Lot Numbers:

1. 11/5/23 2. 11/5/23 3. 11/4/23 4. 11/4/23 5. 11/5/23 6. 11/3/23 and 11/4/23 7. 11/5/23

Distribution:

Distributed in: IL, MN, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0583-2024

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