Bix Produce Mixed Fruit products containing Cantaloupe, Honeydew, and Pineapple. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights: 1. Item # 12192, Fruit, Chunk Mixed 1/2", 20 lb. 2. Item # 12240, Fruit, Chunk Mixed 5 lb. 3. Item # 12245, Fruit, Chunk Mixed 1" 20 lb.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot number / Sales Order #: 1. P2760607-00, P2764334-00, P2765219-00, P2765878-00. 2. P2765875-00. 3. P2765892-00, P5221567-00.
  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:
FreshPoint Bix Produce Company, LLC
Reason for Recall:
Potential Salmonella contamination.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Bix Produce Mixed Fruit products containing Cantaloupe, Honeydew, and Pineapple. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights: 1. Item # 12192, Fruit, Chunk Mixed 1/2", 20 lb. 2. Item # 12240, Fruit, Chunk Mixed 5 lb. 3. Item # 12245, Fruit, Chunk Mixed 1" 20 lb.

Product Codes/Lot Numbers:

Lot number / Sales Order #: 1. P2760607-00, P2764334-00, P2765219-00, P2765878-00. 2. P2765875-00. 3. P2765892-00, P5221567-00.

Distribution:

Distributed in: IA, MN, ND, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0670-2024

Related Recalls