Bean Sprout recall
Recalled by Fuji Natural Foods, Inc. · Ontario, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Fuji Natural Foods, Inc. is voluntarily recalling all Mung Bean Sprout products because they may contain a foreign object.
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
Bean Sprout 10 lbs. bag, 10lb box, 12/12oz, 20/15oz, 24/1.5 lbs., 5lbs. bag, 3lb tray
Quantity: 6,978 units
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.
10 lb bag: 427841 427842 428813 428833 428839 428855 429817 429832 429835 429848 430804 430843 501802 501804 501808 501821 501830 501853 10 lb box: 428813 430832 430843 501802 501824 12/12 oz: 0501A51 0505A12 0505A22 0505A31 0505A41 0505A50 0506A49 0506A63 0507A09 0507A49 0508A04 0508A08 0508A30 0508A45 0509A11 0509A30 0509A40 0510A36 1018A51 1297A35 20/15 oz: 0505A63 0506A09 0506A33 0508A51 24/1.5 lb: 0504A22 0504A31 0504A39 0504A41 0504A50 0504A59 0505A12 0505A33 0505A49 0505A63 0506A35 0507A04 0507A08 0507A09 0507A35 0507A45 0508A11 0508A29 0508A30 0508A40 1018A51 1297A35 5 lb bag: 427812 427822 427831 427841 428817 428854 428863 430811 430830 430840 501811 3 lb tray: 427822 429809 430839
Where it was sold
FDA's distribution note: US
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
- Fuji Natural Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 2, 2017
- In FDA report of
- May 31, 2017
- Terminated
- May 19, 2017
- FDA recall number
- F-2210-2017 · event 77174
- Official record
- FDA enforcement report search