This is the story of the FDA’s persecution of Samuel Girod.


 

 

By Sally Oh on March 1, 2017 | Comments 2 | Affiliate Disclosure

Here’s a video explaining the entire thing, transcript with links below.

Let’s be clear about a couple of pertinent facts:

1. The FDA made up arbitrary rules, then accused Sam of breaking those rules.

2. There are no victims. Samuel Girod has hurt no one.

3. FDA-approved pharmaceutical drugs kill 1 person every 19 minutes. Merck’s FDA-approved Vioxx killed over 68,000 people. Nobody in Big Pharma goes to jail. They pay out billions in fines (after making billions in profits.) No companies close, nobody goes to jail. Nobody. Even after killing and harming 100s of thousands of people.

4. Sam Girod and his products have hurt no one.

The Story of the FDA v Samuel Girod

Samuel Girod and his family have been making and selling 3 all-natural herbal products for nearly 20 years. In all those years, one woman had a bad reaction to a salve (which Sam made right and the woman was fine).

No one has ever been harmed by the products, the Girods have pages of testimonials and scores of repeat customers.

The 3 products are: Original Chickweed, a beeswax, essential oils and olive oil salve; Sine-Eze, a blend of essential oils; and To-Mor-Gone, an herbal bloodroot product in a base of beeswax and olive oil aka “black salve”.

All of these products are currently ALSO made and sold online worldwide (including on Amazon) by other people using these same basic ingredients. The recipes are online as well, you can make them in your kitchen.

HOW IT STARTED

Sixteen years ago, in 2001, an FDA agent visited Sam at his home in IN and informed Sam that he could not claim his products could help skin cancer. At that time, the chickweed salve label said: “[g]ood for all skin disorders. Skin cancer, cuts, burns, draws, and poison ivy.”

According to the FDA, when you make a medical claim about a product, that means the product is a “drug. Therefore you have to do years of testing, costing millions of dollars to prove the claim.

Sam had to change his label or do the testing.

So Sam changed the label, removing the reference to skin cancer.

He asked the agent to get back to him on what label would be acceptable to the FDA. The agent said she would within three weeks but she never did.

The label now said, “[g]ood for skin disorders. Dry skin, cuts, burns, draws, and poison ivy.” No skin cancer reference.

Between 2001 and 2004, Sam was visited several times by FDA agents. When he asked the agents what was acceptable on the label, none would give
an answer.

Sam did not receive any further communication from the FDA until 2012.

In Jan 2012, someone called the FDA and reported that a store in MO was selling Chickweed Healing Salve and that medical claims were being made.

The FDA confiscated the products from the store and opened #Case 4:12-cv-00362-GAF on Sam. You will find a link to the complaint and a link to Sam’s answer in the transcript below.

This is the complaint: http://bit.ly/27-on-120928-Girod-Amended-Complaint

This is Sam’s answer to the complaint: http://bit.ly/37-on-121228-Girod-Answer-Defenses


In fact, here are all the court documents on Sam’s entire case. There are two folders: the 1st is for the labeling, the 2nd is for the criminal indictment.


PLEASE FOLLOW THIS LINK TO THE FULL STORY!

CONTINUE READING AND TO VIDEO HERE!