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 - DangerousWhat Should You Do?
- 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.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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.govFDA Recall Number: F-0670-2024
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