Product Wiki · Recalls · U.S. FDA — Food Enforcement

Wegmans Semi-Sweet Chocolate Nonpareils, NET WT 18.5 OZ (1 LB 2.5 OZ)… — recall H-0278-2025

U.S. FDA — Food Enforcement · United States · 2025-06-16 · Class II

As described by U.S. FDA — Food Enforcement: Wegmans Semi-Sweet Chocolate Nonpareils, NET WT 18.5 OZ (1 LB 2.5 OZ) (524 g), packaged in a plastic tub and packed 12 per case, Distributed by: Wegmans Food Markets, Inc. Rochester, NY 14603. Ingredients: Sugar, Chocolate Liquor, Cacao Fat, Corn Starch, Soy Lecithin (emulsifier), Glazing Agent (Ca

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Food Enforcement
Recall identifier
H-0278-2025
Date of alert
2025-06-16
Country / jurisdiction
United States
Risk level
Class II
Notice type
recall
Brand
Mellace Family Brands California Inc
Product category
food
Product type
Food
Recall status
Terminated — the recall action is complete and the FDA has closed it
Initiated by
Voluntary: Firm initiated
Distribution
Product was distributed to retail stores in: DC, DE, MD, MA, NC, NJ, NY, PA, VA
Barcode (EAN/GTIN)
10077890497873
Reported risk: Undeclared milk
What to do

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from U.S. FDA — Food Enforcement →

Primary source: https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0278-2025%22

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.