Check the Batch
Class ITerminated in FDA datasetRecall initiated Oct 10, 2016

Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz.

Recalling firm: Wells Enterprises, Inc.

Why it was recalled

Product may be contaminated with Listeria Monocytogenes.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 5, 2017.

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Compare the exact product and package details with the label you have.

ProductBlue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
Package size46 fl. oz
UPC070640014644, 070640014651

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).

Extracted codes and context

TypeCode / valueContext
UPC070640014644UPC 070640014644 LOT 60001 MM 19115 6228 BEST IF USED BY 02/13/18; and UPC 070640014651 (High altitude) LOT 60001 MM 19115 6229
UPC070640014644Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
UPC070640014651UPC 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
UPC070640014651unny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
best by02/13/18UPC 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
best by02/14/18 UPC 070640014651 (High altitude) LOT 60001 MM 19115 6229 BEST IF USED BY 02/14/18

Original FDA recall reason

Product may be contaminated with Listeria Monocytogenes.

Recall details

Recall number
F-0479-2017
Event ID
75405
FDA status
Terminated
Initiated
Oct 10, 2016
Reported
Nov 30, 2016
Classified
Nov 18, 2016
Terminated
Jan 5, 2017
Quantity
7192 cases
Location
Le Mars, IA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Product was distributed to NE, OK, KS, MO, AZ, and TX.

FDA source record · F-0479-2017

Data updated September 16, 2026. View official FDA data ↗

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