Jack and the Beanstalk Soybean Sprouts and Natto Sprouts; Packaged in 1 lb., 1.5 lb. and 10 lb. packages. and Natto Soybean sprouts pack...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1435-2015.
Positive results of FDA sampling for Listeria Monocytogenes - environmental and finished product..
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1435-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Hanbit Enterprises, Inc. Dba Jack And The Beanstalk or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1435-2015.
Hanbit Enterprises, Inc. dba Jack and the Beanstalk
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Hanbit Enterprises, Inc. Dba Jack And The Beanstalk Recall FAQ
Hanbit Enterprises, Inc. Dba Jack And The Beanstalk is the subject of a food safety report: Jack and the Beanstalk Soybean Sprouts and Natto Sprouts; Packaged in 1 lb., 1.5 lb. and 10 lb. packages. and Natto Soybean sprouts pack.... The notice was published on February 13, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 410 units are potentially affected.