YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4
Reason Incorrect overwrap leads product to contain undeclared peanuts and eggs.
Light & Fit¿ Greek Crunch Nonfat Yogurt & Toppings S Mores Flavor recall
Recalled by Danone Waters of America INC · White Plains, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Danone North America is voluntarily recalling Light & Fit¿ Greek Crunch Nonfat Yogurt & Toppings S Mores Flavor because it was discovered that some of the toppers sold on the product contain peanuts and are improperly labeled.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
LIGHT & FIT¿ GREEK CRUNCH NONFAT YOGURT & TOPPINGS S MORES FLAVOR, 5 oz Preformed cups with a topper, Refrigeration required between 36F and 45F, UPC 36632 03825
Quantity: 3,521 cases
Food: Milk & dairy
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.
Date Code DEC 30 2018 49-64 WP
Where it was sold
Connecticut Iowa Illinois Massachusetts Maryland Michigan Missouri New Jersey New York Ohio Pennsylvania Texas Virginia Wisconsin
FDA's distribution note: 13 states: Connecticut, Illinois, Iowa, Maryland, Massachusetts, Michigan, Missouri, New Jersey, New York, Ohio, Pennsylvania, Texas,Wisconsin. No foreign or govt/VA/military consignees.
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. 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
- Danone Waters of America INC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 5, 2018
- In FDA report of
- Dec 26, 2018
- Terminated
- Mar 11, 2019
- FDA recall number
- F-0740-2019 · event 81722
- Official record
- FDA enforcement report search
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