CLASS I Food recall · Reported 5 Nov 2014 · FDA Enforcement Report

WildForce Green Formula, The Power of Wild Plants bottles recalled

Herb Garden Productions is recalling WildForce Green Formula, The Power of Wild Plants bottles in 2500cc food grade white, distributed in Nevada. The recall was initiated on 14 Oct 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT#: 821010-009 EXP.:06/2015 Manufacture Date: 06/2014 UPC CODE: 96859201233
Quantity recalled1000 x 430 gram. containers.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0082-2015
FDA event ID
69510
Recalling firm
Herb Garden Productions, Las Vegas, NV
Classification
Class I
Status
Terminated
Recall initiated
14 Oct 2014
FDA classified
27 Oct 2014
Reported
5 Nov 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Salmonella
Product category
Herbal Supplements

Timeline

14 Oct 2014Recall initiated by company
27 Oct 2014Classified by FDA+13 days
5 Nov 2014Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Notified by immediate supplier that Nettle Leaf Powder may contain Salmonella after reports of a positive finding by a customer.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

WildForce Green Formula, The Power of Wild Plants, 430 grams. bottles in 2500cc food grade white plastic bottle. Manufacturer: Herbally Grounded LLC., Curtiss Harris 7023640090 3744 W. Meade Ave. Ste. 11a Las Vegas, NV 89102

Where it was distributed

NV and internet sales.

Nevada

Questions about this recall

Why was it recalled?

Notified by immediate supplier that Nettle Leaf Powder may contain Salmonella after reports of a positive finding by a customer.

Which lots are affected?

LOT#: 821010-009 EXP.:06/2015 Manufacture Date: 06/2014 UPC CODE: 96859201233

Where was it sold?

NV and internet sales.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 69510

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