Werner Brand Butter Toffee Peanuts, net wt. 2.25 oz, UPC 7 09972 80113 3 Werner Brand Butter Toffee Peanuts, net wt. 6 oz., UPC 7 09972 80027 3 The ingredients statement declared: Peanuts, Sugar, Butter, Salt. The label contains an advisory statement Allergen Information: "***This product is manufactured and packaged on shared equipment and may contain: Peanuts, Tree Nuts, Soy, Wheat, Milk or Eggs***".

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Best By Jan. 29, 2017 or before
  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:
Werner Gourmet Meat Snacks, Inc.
Reason for Recall:
Werner Brand Butter Toffee Peanuts are recalled because the labels declared butter, but milk is not declared.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Werner Brand Butter Toffee Peanuts, net wt. 2.25 oz, UPC 7 09972 80113 3 Werner Brand Butter Toffee Peanuts, net wt. 6 oz., UPC 7 09972 80027 3 The ingredients statement declared: Peanuts, Sugar, Butter, Salt. The label contains an advisory statement Allergen Information: "***This product is manufactured and packaged on shared equipment and may contain: Peanuts, Tree Nuts, Soy, Wheat, Milk or Eggs***".

Product Codes/Lot Numbers:

Best By Jan. 29, 2017 or before

Distribution:

Distributed in: AK, CA, CO, CT, ID, KS, MA, MN, MT, NJ, NM, NV, NY, OK, OR, SC, TX, VA, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1417-2016

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