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Class I: serious health riskCompleted

SunOpta Food and Grain 2nd EXPANSION 5/31/2016 Product shipped OUS Recall

2nd EXPANSION 5/31/2016 Product shipped OUS only

SunOpta Food and Grain, Inc. · Crookston, MN

Risk level
Class I
Reported by FDA
Sep 21, 2016
Recall ID
F-2265-2016
Check your lot numberHow we source this data

Summary

SunOpta Food and Grain recalled 2nd EXPANSION 5/31/2016 Product shipped OUS starting May 2, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-2265-2016 on Sep 21, 2016. Reason: 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. Status: Completed.

Why it 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

Product description

2nd EXPANSION 5/31/2016 Product shipped OUS only. Light Salt Sunflower Kernel, 5 kg / 11 lb. box. Product of USA, Manufactured by SunOpta, Crookston, MN

Lot numbers, UPCs & expiration codes

2nd EXPANSION 5/31/2016 PLot#: 8L5M10

Where it was sold

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.

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-2265-2016
Classification
Class I
Status
Completed
Recall initiated
May 2, 2016
FDA report date
Sep 21, 2016
Quantity
2nd EXPANSION 5/31/2016 8,266,463 lbs. total
Recall type
Voluntary: Firm initiated
Recalling firm
SunOpta Food and Grain, Inc.

Original FDA data

Every field from FDA enforcement report F-2265-2016, exactly as published.

Show all FDA fields
City
Crookston
State
MN
Status
Completed
Country
United States
Event ID
74020
Address
1220 Sunflower St
Code information
2nd EXPANSION 5/31/2016 PLot#: 8L5M10
Postal code
56716-2480
Report date
Sep 21, 2016
Product type
Food
Recall number
F-2265-2016
Classification
Class I
Recalling firm
SunOpta Food and Grain, Inc.
Product quantity
2nd EXPANSION 5/31/2016 8,266,463 lbs. total
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
Voluntary / mandated
Voluntary: Firm initiated
Product description
2nd EXPANSION 5/31/2016 Product shipped OUS only. Light Salt Sunflower Kernel, 5 kg / 11 lb. box. Product of USA, Manufactured by SunOpta, Crookston, MN
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.
Recall initiation date
May 2, 2016
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Sep 15, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2265-2016, published Sep 21, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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