Why it was recalled
Product may be contaminated with Listeria Monocytogenes.
Product description
Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
Lot numbers, UPCs & expiration codes
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
Product was distributed to NE, OK, KS, MO, AZ, and TX.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0479-2017
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Oct 10, 2016
- FDA report date
- Nov 30, 2016
- Quantity
- 7192 cases
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Wells Enterprises, Inc.
Original FDA data
Every field from FDA enforcement report F-0479-2017, exactly as published.
Show all FDA fields
- City
- Le Mars
- State
- IA
- Status
- Terminated
- Country
- United States
- Event ID
- 75405
- Address
- 1 Blue Bunny Dr SW
- Address (line 2)
- PO Box 1310
- 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
- Postal code
- 51031-2207
- Report date
- Nov 30, 2016
- Product type
- Food
- Recall number
- F-0479-2017
- Classification
- Class I
- Recalling firm
- Wells Enterprises, Inc.
- Product quantity
- 7192 cases
- Termination date
- Jan 5, 2017
- Reason for recall
- Product may be contaminated with Listeria Monocytogenes.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
- Distribution pattern
- Product was distributed to NE, OK, KS, MO, AZ, and TX.
- Recall initiation date
- Oct 10, 2016
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Nov 18, 2016