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Honey Bunchies Gourmet Honey Bars, 1.9 oz. snack bar containing honey, sunflo...

FDA Recall #F-1871-2016 — Class I — May 31, 2016

Recall Summary

Recall NumberF-1871-2016
Date InitiatedMay 31, 2016
ClassificationClass I
StatusTerminated
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmHoney Bunchie, LLC
LocationLongmont, CO

Product Description

Honey Bunchies Gourmet Honey Bars, 1.9 oz. snack bar containing honey, sunflower kernels, peanuts and pecans. Packaging: Box containing 20 individual bars in plastic wrappers. Manufactured by: Honey Bunchie, LLC, Longmont, CO. Individual Bar UPC 8 66192 00010 1; Box of 20 Bars UPC 8 66192 00011 8.

Reason for Recall

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.

Classification

Class I — A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.

Distribution Pattern

Nationwide. No foreign/govt/VA/military consignees.

Product Quantity

45, 960 bars

Product Codes / Lot Numbers

Lot Production Date Best Buy Date D4 7/27/2015 12/27/2015 E4 7/28/2015 12/28/2015 F4 8/03/2015 1/03/2016 G4 8/04/2015 1/04/2016 H4 8/10/2015 1/10/2016 I4 8/18/2015 1/18/2016 J4 8/24/2015 1/24/2016 K4 8/26/2015 1/26/2016 L4 8/31/2015 1/31/2016 M4 9/07/2015 4/07/2016 N4 9/14/2015 4/14/2016 O4 9/21/2015 4/21/2016 P4 9/22/2015 4/22/2016 Q4 9/28/2015 4/28/2016 R4 10/05/2015 5/05/2016 S4 10/05/2015 8/05/2016 T4 10/12/2015 5/12/2016 U4 10/12/2015 8/12/2016 V4 10/19/2015 8/19/2016 W4 10/20/2015 8/20/2016 X4 10/26/2015 8/26/2016 Y4 11/03/2015 9/03/2016 Z4 11/09/2015 9/09/2016 A5 11/16/2015 9/16/2016 B5 11/23/2015 9/23/2016 C5 11/30/2015 9/30/2016 D5 12/07/2015 10/07/2016 E5 12/14/2015 10/14/2016 F5 12/21/2015 10/21/2016 G5 12/28/2015 10/28/2016

What Should You Do?

Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.

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Frequently Asked Questions

Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.

Listeria monocytogenes is one of the most serious foodborne pathogens. Unlike most bacteria, Listeria can grow at refrigerator temperatures (below 40°F), meaning refrigerating a contaminated product does not stop the risk. Symptoms can appear 1 to 4 weeks after eating contaminated food and may include fever, muscle aches, headache, stiff neck, confusion, and loss of balance. Listeriosis is particularly dangerous for pregnant women — infection can cause miscarriage, stillbirth, or premature delivery. If you consumed this recalled product and are in a high-risk group (pregnant, elderly, or immunocompromised), contact your doctor immediately even if you feel well.

Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.

The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.

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