Waffle Works Double Chocolate Waffle Sandwich Snacks Net Wt. 4 OZ.. Distributed By: Herr Foods, Inc., Nottingham, PA 19363. June0616 t...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1700-2016.
Packaging failed to declare the milk ingredient (whey powder) in the ingredient statement. The allergen statement listed Wheat and Soy Ingredients, but did not include Milk Ingredients (whey powder).
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1700-2016.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Herr Foods, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-1700-2016.
Herr Foods, Inc.
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.
Herr Foods, Inc. Recall FAQ
Herr Foods, Inc. is the subject of a snacks & candy safety report: Waffle Works Double Chocolate Waffle Sandwich Snacks Net Wt. 4 OZ.. Distributed By: Herr Foods, Inc., Nottingham, PA 19363. June0616 t.... The notice was published on June 6, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 84,528 units are potentially affected.