Bertagni fresh Sweet Butternut Squash Ravioli, packaged in a paper tray inside a plastic bag and wrapped around with paper band, net weight 8.8 oz., UPC 8001020110139.

Class I - Dangerous
Recalled: November 17, 2015 Bertagni 1882 Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Expiration dates from 8/3/16 to 1/29/17. Lot codes: 506B, 508C, 511D, 512C, 513B, 516B, 520A, 522B, 522F, 523B, 523C, 529C, 530F, 531F, 535C, and 536A. The lot code is interpreted as below: Example 506B: 5=2015; 06= week 6 of the year; B= second day of the week (Tuesday)
  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:
Bertagni 1882
Reason for Recall:
Bertagni fresh Sweet Butternut Squash Ravioli is recalled because the products may contain undeclared cashew and almond.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Bertagni fresh Sweet Butternut Squash Ravioli, packaged in a paper tray inside a plastic bag and wrapped around with paper band, net weight 8.8 oz., UPC 8001020110139.

Product Codes/Lot Numbers:

Expiration dates from 8/3/16 to 1/29/17. Lot codes: 506B, 508C, 511D, 512C, 513B, 516B, 520A, 522B, 522F, 523B, 523C, 529C, 530F, 531F, 535C, and 536A. The lot code is interpreted as below: Example 506B: 5=2015; 06= week 6 of the year; B= second day of the week (Tuesday)

Distribution:

Distributed in: CA, IL, MI, MN, NY, OH, OR, IN, KY, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1043-2016

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