Mungbean Sprouts net wt
Reason Mungbean Sprouts are recalled because finished product was tested positive for Listeria monocytogenes.
Soybean Sprouts net wt recall
Recalled by Kkot Saem Bean Sprouts · Spanaway, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Soybean Sprouts are recalled because it has the potential to be contaminated with Listeria monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Soybean Sprouts, net wt. 1.5 lbs., sold under brand Winter Blossom Bean Sprouts brand. Product is packaged in plastic bag, multi-colored with orange stripe on top, lower middle portion and at bottom. The orange & black English and Korea letters on white background on front of bag. the UPC is 0 94922 55330 0. Soybean Sprouts, net wt. 5 lbs., sold in clear bag with no label. There is no UPC for this product.
Quantity: 8851.5 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.
None
Where it was sold
Oregon Washington
FDA's distribution note: Distributed in Oregon and Washington
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Kkot Saem Bean Sprouts
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 19, 2014
- In FDA report of
- Feb 18, 2015
- Terminated
- Jun 23, 2015
- FDA recall number
- F-1025-2015 · event 70072
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.