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CriticalFDAfda-F-1985-2017UNDECLARED ALLERGEN

Wegmans Milk Chocolate Sucker, NET WT 3 OZ. The product is shipped within a carton labeled with an orange label as WEGMANS SWISS RECIPE...

⚠ 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.

Category
Units Affected
72
Recall Date
March 6, 2017
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1985-2017.

Contains Undeclared Peanuts

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1985-2017.

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 Landies Candies, 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-1985-2017.

Landies Candies, Inc.

FDA

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

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📣 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.

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Landies Candies, Inc. Recall FAQ

Landies Candies, Inc. is the subject of a dairy safety report: Wegmans Milk Chocolate Sucker, NET WT 3 OZ. The product is shipped within a carton labeled with an orange label as WEGMANS SWISS RECIPE.... The notice was published on March 6, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 72 units are potentially affected.