Jack and the Beanstalk Soybean Sprouts and Natto Sprouts recall
Recalled by Hanbit Enterprises, Inc. dba Jack and the Beanstalk · Salinas, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Positive results of FDA sampling for Listeria Monocytogenes - environmental and finished product..
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
Jack and the Beanstalk Soybean Sprouts and Natto Sprouts; Packaged in 1 lb., 1.5 lb. and 10 lb. packages. and Natto Soybean sprouts packed in 396 g. plastic bags
Quantity: approximately 410 boxes ( 20 bags per box)
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.
1LB SOYBEAN SPROUT BAR CODE 727580¿123669; 1.5LB SOYBEAN SPROUT BAR CODE 7¿27580-123652; 10LB SOYBEAN SPROUT BAR CODE - 7¿27580-12351-5 NATTO SOYBEAN SPROUT BAR CODE- 7¿27580-¿12367¿6 All best by dates up to and including February 12, 2015.
Where it was sold
California
FDA's distribution note: CA only to markets and restaurants
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
- Hanbit Enterprises, Inc. dba Jack and the Beanstalk
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 13, 2015
- In FDA report of
- Mar 25, 2015
- Terminated
- Mar 30, 2015
- FDA recall number
- F-1435-2015 · event 70525
- Official record
- FDA enforcement report search