WildForce Green Formula, The Power of Wild Plants, 430 grams. bottles in 2500cc food grade white plastic bottle. Manufacturer: Herb...
⚠ 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-0082-2015.
Notified by immediate supplier that Nettle Leaf Powder may contain Salmonella after reports of a positive finding by a customer.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0082-2015.
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 Herb Garden Productions 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-0082-2015.
Herb Garden Productions
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.
Herb Garden Productions Recall FAQ
Herb Garden Productions is the subject of a baby food & formula safety report: WildForce Green Formula, The Power of Wild Plants, 430 grams. bottles in 2500cc food grade white plastic bottle. Manufacturer: Herb.... The notice was published on October 14, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 1,000 units are potentially affected.