2nd EXPANSION 5/31/2016 Roasted No Salt Sweet Onion & White Cheddar Sunflowe...

FDA Recall #F-2267-2016 — Class I — May 2, 2016

Recall Summary

Recall NumberF-2267-2016
Date InitiatedMay 2, 2016
ClassificationClass I
StatusCompleted
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmSunOpta Food and Grain, Inc.
LocationCrookston, MN

Product Description

2nd EXPANSION 5/31/2016 Roasted No Salt Sweet Onion & White Cheddar Sunflower Kernel, 45 lb. box. Product of USA, Manufactured by SunOpta, Crookston, MN

Reason for Recall

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

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

AR, CA, CO, IL, IN, KY, MN, NC, ND, NH, OH, PA, SD, TX, WA, WI. EXPANDED 5/18/2016 Additional states: CT, FL, GA, IA, KS, LA, MA, MI, NJ, NY, OR 2nd EXPANSION 5/31/2016 Additional States: MD, MT, OK, VA. OUS to include: Canada, GUATEMALA, Great Britain, and Mexico.

Product Quantity

2nd EXPANSION 5/31/2016 8,266,463 lbs. total

Product Codes / Lot Numbers

2nd EXPANSION 5/31/2016 PLot#: 8H5M26

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.

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.