For Immediate Release
June 13, 2016
Longmont, CO. — Honey Bunchie, LLC is initiating a voluntary recall of a limited number of Honey Bunchies Gourmet Honey Bars that contain SunOpta sunflower kernels that have the potential of contamination with Listeria monocytogenes.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products were distributed directly from Honey Bunchie, LLC to distributors, retailers and online consumers between 08/05/2015 – 03/15/2016.
To date, Honey Bunchie, LLC has not received any reports of illness; however, the company is initiating this voluntary recall in an abundance of caution as part of its commitment to the health and safety of its consumers.
Product Name: Honey Bunchies Gourmet Honey Bar
|Description||UPC Code||Size||Best By Date|
|Individual Bar||8 66192 00010 1||1.9 oz||12/27/2015 – 10/28/2016|
|Box of 20 Bars||8 66192 00011 8||20 bars, 1.9 oz each||12/27/2015 – 10/28/2016|
No other products produced by Honey Bunchie, LLC are affected by this recall.
The affected bars were sold nationwide through distributors, retailers and online.
Consumers who have purchased affected product are urged not to consume the product and return it to the place of purchase for a full refund. Online customers should contact the company at email@example.com. Consumers with questions may contact the company at (303) 808-3351.
Retailers and wholesale customers should check their inventories and shelves to confirm none of the affected products are present or available for purchase by consumers or in warehouse inventories. Please contact Honey Bunchie at firstname.lastname@example.org to arrange for disposal or return of the product.
This recall is being made with the knowledge of the Food and Drug Administration.