Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
Wegmans Milk Chocolate Sucker recall
Recalled by Landies Candies, Inc. · Buffalo, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Contains Undeclared Peanuts
Undeclared allergen: Peanut
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Wegmans Milk Chocolate Sucker, NET WT 3 OZ. The product is shipped within a carton labeled with an orange label as WEGMANS SWISS RECIPE Milk Chocolate Big Ear Bunny Sucker (3 oz 36 count case). The individual product contains a lavender label and read Wegmans Milk Chocolate Sucker, comes in a 3-oz., clear plastic flow wrap 6 long by 2 wide.
Quantity: 72 units
Food: Chocolate & candy
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot #35016 Best by 9-15-2017
Where it was sold
New York
FDA's distribution note: New York region through Wegman's Stores
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Landies Candies, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 6, 2017
- In FDA report of
- Apr 26, 2017
- Terminated
- Jul 9, 2018
- FDA recall number
- F-1985-2017 · event 76657
- Official record
- FDA enforcement report search
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