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RECALL RECORD — CLASS IIRecall closedF-1769-2012/FDA enforcement
Sunopta Ingredients Group (Corporate Hq)·Food·Jun 8, 2012

Sunopta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by Sunopta Ingredients, …

What you need to know

Class II

  • What happened

    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…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDADistribution not listedMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameSunopta Ingredients Group (Corporate Hq)
Recalling firmSunopta Ingredients Group (Corporate Hq)Chelmsford, MA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • 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
Distribution area

Arizona, Michigan, Virginia, and Holland Recall expanded on 6/19/12 to include California.

United States

Quantity affected48, 750 lbs. 6/21 EXPANDED 27, 300 lbs. 6/26 EXPANDED 3900 lbs.
Recall initiationFDA report date: July 25, 2012
FDA recall numberF-1769-2012

Beyond the headline

The recall, in context

Sunopta Ingredients Group (Corporate Hq) initiated this food recall on June 8, 2012. The FDA enforcement report states: 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. The FDA report lists distribution as: Arizona, Michigan, Virginia, and Holland Recall expanded on 6/19/12 to include California.

The FDA enforcement report describes the reason as: 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.

Sunopta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by Sunopta Ingredients, … was made or distributed by Sunopta Ingredients Group (Corporate Hq) in Chelmsford, MA, United States. This page reflects FDA report F-1769-2012, dated July 25, 2012.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Sunopta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by Sunopta Ingredients, … recall?

Sunopta Ingredients Group (Corporate Hq) recalled Sunopta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by Sunopta Ingredients, … in an FDA Class II enforcement action reported as F-1769-2012. 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…

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Sunopta Ingredients Group (Corporate Hq) recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1769-2012. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.