Skip to main content
High RiskFDAfda-F-1418-2016UNDECLARED ALLERGEN

Werner Brand Sweet Hot Crunch Mix, net wt. 2 oz, UPC 7 09972 80120 1. Werner Brand Sweet Hot Crunch Mix, net wt. 6 oz, UPC 7 09972 80100...

Category
Units Affected
24,318
Recall Date
May 2, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1418-2016.

Werner Brand Sweet Hot Crunch Mix is recalled because label declared butter, but milk is not declared.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1418-2016.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Werner Gourmet Meat Snacks, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1418-2016.

Werner Gourmet Meat Snacks, Inc.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Werner Gourmet Meat Snacks, Inc. Recall FAQ

Werner Gourmet Meat Snacks, Inc. is the subject of a dairy safety report: Werner Brand Sweet Hot Crunch Mix, net wt. 2 oz, UPC 7 09972 80120 1. Werner Brand Sweet Hot Crunch Mix, net wt. 6 oz, UPC 7 09972 80100.... The notice was published on May 2, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 24,318 units are potentially affected.