Recall record at a glance
| Official record | F-2269-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Completed |
| Recalling firm | SunOpta Food and Grain, Inc. |
| Report date | Sep 21, 2016 |
| Recall initiation date | May 2, 2016 |
| Quantity | 2nd EXPANSION 5/31/2016 8,266,463 lbs. total |
| Location | Crookston, MN, United States |
Official product description
2nd EXPANSION 5/31/2016 Sunrich Naturals Chili Lime flavored Sunflower Kernels, packaged under the following sizes: 1. Net Wt. 1 oz. plastic bag, UPC 10304-01214; 2. Net Wt. 1.2 oz. (34g), UPC 10304-03214 . Product of USA. Distributed by Sunrich Consumer Brands, Hope, MN 56046
Why the product was recalled
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
Distribution information
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.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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