Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 8, 2020 (7 years ago)

Organic IntegriPure Cold Milled Flaxseed recall

Recalled by Healthy Food Ingredients, LLC · Fargo, ND, United States

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

Why it was recalled

Product is being recalled due to detection of an unapproved herbicide.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Organic IntegriPure Cold Milled Flaxseed, 50 lb Net Wt. and 2000 lb. totes

Quantity: 74,500 lbs. EXPANDED 02/2020 257,083 lbs.

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.

Lots: 4P194M-041119-103, 4P197M-270919-103, 4P197M-241019-EC. EXPANDED February 2020: Lot numbers: 4P152M-300719-103, 4P152M-300719-EC, 4P154M-120619-103, 4P154M-210619-101, 4P154M-EC, 4P155M-120619-103, 4P155M-120619-EC, 4P172M-300719-103, 4P172M-300719-EC, 4P179M-190819-103, 4P180M-311019-103, 4P190M-311219-103, 4P191M-170919-103, 4P191M-301219-EC, 4P203M-151019-101.

Where it was sold

California Colorado Minnesota Missouri North Carolina Nebraska Pennsylvania Rhode Island Utah Wisconsin

FDA's distribution note: CA, CO, UT. EXPANDED February 2020: MN, MO, NC, NE, PA, RI, WI. International distribution to Canada

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
Healthy Food Ingredients, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 8, 2020
In FDA report of
Feb 5, 2020
Terminated
Jul 6, 2022
FDA recall number
F-0571-2020 · event 84675
Official record
FDA enforcement report search

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