Woodland Gourmet Arrowroot Flour item code H59EE86
Reason Possible presence of Foreign Material
Woodland Ingredients X06D Arborio Rice recall
Recalled by Woodland Foods LLC · Waukegan, IL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
possible presence of glass pieces
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice, 25 lbs. bag UPC 00687080069143 Sysco International X06D05 Arborio Rice, 25 lbs. bag in box UPC 00074865718257 DGourmet.com X06C Arborio Rice, 10 lbs. bag in box UPC 00687080007367
Quantity: 2299 bags (50235 pounds)
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.
Lot #'s 2317128 2317772 2316634 2317098 2322970 2319588 2321998 2321011 2326070 2321214
Where it was sold
Arizona California Connecticut Florida Georgia Illinois Indiana Massachusetts Maine Michigan Minnesota Missouri Montana North Carolina New Hampshire New Jersey New York Ohio South Dakota Texas Virginia Washington Wisconsin
FDA's distribution note: AZ CA CT FL GA IL IN MA ME MI MN MO MT NC NH NJ NY OH SD TX VA WA WI
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
- Woodland Foods LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 13, 2022
- In FDA report of
- Sep 7, 2022
- Terminated
- May 15, 2023
- FDA recall number
- F-1581-2022 · event 90609
- Official record
- FDA enforcement report search
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