next by Nature brand DARK CHOCOLATE CHERRIES
Reason Next by Nature brand Dark Chocolate Cherries Lot 460013 may contain undeclared peanuts (from bulk product).
next by Nature brand DARK CHOCOLATE BANANAS recall
Recalled by Tropical Valley Foods, Inc. · Plattsburgh, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The product contains the undeclared allergens walnuts and milk.
Undeclared allergens: Milk Tree nuts
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
next by Nature brand DARK CHOCOLATE BANANAS, NET WT. 3 Oz. (85g), UPC 8 17582 25600 4, Produced by Tropical Valley Foods
Quantity: N/A
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.
"Best by Date" of 12/18/2013 and 12/19/2013
Where it was sold
Colorado Michigan New Jersey Oregon
FDA's distribution note: Michigan, Oregon, Colorado, and New Jersey
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 milk, tree nuts; 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
- Tropical Valley Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 12, 2013
- In FDA report of
- Jun 5, 2013
- Terminated
- May 4, 2017
- FDA recall number
- F-1458-2013 · event 65203
- Official record
- FDA enforcement report search
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