Plastic 1-gallon clear pail blue label which reads in part as…
Reason Elevated coliforms
Blue Bunny Ice Cream Hoppin' Holidoodle ice cream recall
Recalled by Wells Enterprises, Inc. · Le Mars, IA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may be contaminated with Listeria Monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
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
Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
Quantity: 7192 cases
Food: Ice cream
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.
UPC 070640014644 LOT 60001 MM 19115 6228 BEST IF USED BY 02/13/18; and UPC 070640014651 (High altitude) LOT 60001 MM 19115 6229 BEST IF USED BY 02/14/18
Where it was sold
Arizona Kansas Missouri Nebraska Oklahoma Texas
FDA's distribution note: Product was distributed to NE, OK, KS, MO, AZ, and TX.
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
- Wells Enterprises, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 10, 2016
- In FDA report of
- Nov 30, 2016
- Terminated
- Jan 5, 2017
- FDA recall number
- F-0479-2017 · event 75405
- Official record
- FDA enforcement report search
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