SunOpta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by SunOpta Ingredients, Chelmsford, MA 01824

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    22211314AA 22211315AA 22211316AA 22211317AA and 22211318AA was reworked into Lots 22211339DD, 22211342DD, 22211343DD, 22211344DD, 22211346DD, 22211347DD, and 22211350DD EXPANDED 06/21/2012 to include more lots: 22211311AA, 22211312AA, 22211313AA, 22211353DD EXPANDED 06/26/2012 to include more lots: 22211354DD
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
SunOpta Ingredients Group (Corporate HQ)
Reason for Recall:
SunOpta Ingredients Group, Cambridge, MN is voluntarily withdrawing from the market a number of lots of Canadian Harvest¿ Oat Fiber 300-33 because of the possible contamination caused by Cronobactor sakazakii.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

SunOpta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by SunOpta Ingredients, Chelmsford, MA 01824

Product Codes/Lot Numbers:

22211314AA 22211315AA 22211316AA 22211317AA and 22211318AA was reworked into Lots 22211339DD, 22211342DD, 22211343DD, 22211344DD, 22211346DD, 22211347DD, and 22211350DD EXPANDED 06/21/2012 to include more lots: 22211311AA, 22211312AA, 22211313AA, 22211353DD EXPANDED 06/26/2012 to include more lots: 22211354DD

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1769-2012

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