Italian Cheese Blend packaged in the following configurations: 1. Sargento Part #23613, Fancy Shredded Italian Cheese Blend Pack Size 500/0.5 oz. Material #10000946, UPC 46100344583. 2. Sargento Fancy Shredded Italian Cheese Blend. Pack Size 400/1 oz. Net Wt 25.000 lbs. Material #10003284, UPC 46100355343. Keep Refrigerated. Product of USA. Distributed By Sargento Foods Inc, Plymouth, WI 53073 USA.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Batch / Use By Dates: Product 1 02225878 / Best By MAY/02/24 Product 2 02225889 / Best By MAY/02/24
- 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:
- Sargento Foods, Inc.
- Reason for Recall:
- 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 Cheese Blend packaged in the following configurations: 1. Sargento Part #23613, Fancy Shredded Italian Cheese Blend Pack Size 500/0.5 oz. Material #10000946, UPC 46100344583. 2. Sargento Fancy Shredded Italian Cheese Blend. Pack Size 400/1 oz. Net Wt 25.000 lbs. Material #10003284, UPC 46100355343. Keep Refrigerated. Product of USA. Distributed By Sargento Foods Inc, Plymouth, WI 53073 USA.
Product Codes/Lot Numbers:
Batch / Use By Dates: Product 1 02225878 / Best By MAY/02/24 Product 2 02225889 / Best By MAY/02/24
Distribution:
Distributed in: AZ, CA, FL, GA, IL, IN, MD, NC, NJ, NV, OH, RI, TX, WA, WI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1017-2024
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