Kudzu Root (Pueraria montana var. lobata), This product was packaged in a clear plastic bag or poly-woven bags sold in bulk form net weig...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). 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-0892-2020.
Salmonella
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0892-2020.
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 Mountain Rose Inc. Dba Mountain Rose Herbs 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-0892-2020.
Mountain Rose Inc. dba Mountain Rose Herbs
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.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
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.
Mountain Rose Inc. Dba Mountain Rose Herbs Recall FAQ
Mountain Rose Inc. Dba Mountain Rose Herbs is the subject of a supplements safety report: Kudzu Root (Pueraria montana var. lobata), This product was packaged in a clear plastic bag or poly-woven bags sold in bulk form net weig.... The notice was published on March 16, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 24,247 units are potentially affected.