Horizon Organic ORG ASEP CHOC MILK 1%
Reason Product has the potential to be spoiled.
20/20 LifeStyles Yogurt Peanut Crunch Bar recall
Recalled by Pro Sports Club · Bellevue, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product is recalled due to a potential contamination with E. coli O157:H7.
Pathogen: E. coli
Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
20/20 LifeStyles Yogurt Peanut Crunch Bar. Bar UPC 7 8571 00052. Each bar has net weight 2 oz. Box UPC 7 8571 00053. Each box has 12/2 oz. bars. Case UPC 78571 00054. Each case has 12 boxes and it is for shipment only and not for resale.
Quantity: 36,957 bars (2 oz. per bar).
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.
B.B. 22JUL17 2046 This lot means Best By July 22, 2017 and Julian date 2046 represents the production date.
Where it was sold
Washington
FDA's distribution note: Distributed in WA and sold to internet customers through www.2020lifestyles.com.
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
- Pro Sports Club
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 20, 2017
- In FDA report of
- Apr 19, 2017
- Terminated
- Jul 11, 2019
- FDA recall number
- F-1913-2017 · event 76799
- Official record
- FDA enforcement report search
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