Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 8, 2012 (14 years ago)

SunOpta Canadian Harvest Oat Fiber recall

Recalled by SunOpta Ingredients Group (Corporate HQ) · Chelmsford, MA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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

Quantity: 48,750 lbs. 6/21 EXPANDED 27,300 lbs. 6/26 EXPANDED 3900 lbs.

Food: Pasta, rice & grains

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Arizona California Michigan Virginia

FDA's distribution note: Arizona, Michigan, Virginia, and Holland Recall expanded on 6/19/12 to include California.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
SunOpta Ingredients Group (Corporate HQ)
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 8, 2012
In FDA report of
Jul 25, 2012
Terminated
Nov 19, 2013
FDA recall number
F-1769-2012 · event 62323
Official record
FDA enforcement report search

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