NYS Halts 13 Makers of Devil's Claw Supplements Marketed to Arthritis Sufferers

 


New York Botanical Garden study found “Devil’s Claw” supplements from 14 U.S. manufacturers contained the wrong plant. NYS Attorney General Schneiderman announced today that his office issued letters demanding that 13 dietary supplement manufacturers cease and desist from the sale, distribution, or marketing of adulterated or misbranded «devil›s claw» supplements. The letters, sent Wednesday, are based on a study from the New York Botanical Garden that used an advanced DNA barcoding technique to conclude that the devil’s claw supplements from these manufacturers contained a cheaper related species that is considered less desirable. Attorney General Schneiderman requested that the companies furnish proposals, where appropriate, for recalling any adulterated devil’s claw supplements, compensating consumers who purchased the mislabeled products, and reforming their approach to quality control.  

Attorney General Schneiderman also announced that his office has reached an accord with a 14th manufacturer, Nature’s Way, to improve the manufacturing and marketing of its devil’s claw supplements. Nature’s Way committed to ensure that its devil claw’s supplements solely contain the proper plant species and are labeled accordingly. As more fully explained below, Nature’s Way will also refund New York consumers who purchased devil’s claw supplements and continue to extend DNA barcode testing across its herbal product lines with one or two ingredients—one of the first companies in the supplements industry to do so.

Devil’s claw is the commercial name in the United States for the plant Harpagophytum procumbens, which is marketed by the dietary supplement industry as a treatment for arthritis and other forms of joint pain. The purported therapeutic benefits of devil’s claw are not generally accepted in the medical community or approved by the FDA. Native to the Kalahari Desert, there have long been reports of suppliers mixing or substituting devil’s claw with a related plant, Harpagophytum zeyheri, which contains some—but not all—of the same chemicals. Some of the most sought-after chemicals tend to naturally occur in different ratios and in lower concentrations in zeyheri, which is the cheaper of the two plants.

The New York Botanical Garden tested 18 devil’s claw supplements labeled for U.S. sale. The study found that for the 16 supplements for which DNA could be identified, all contained zeyheri, either by itself (81%) or mixed with procumbens (19%).

Attorney General Schneiderman’s cease-and-desist letters target 13 manufacturers, which produced 15 of the test products. These companies include:

Nutraceutical International Corporation (Soloray);

Alternative Remedies Health & Herbs;

The Kroger Co., as parent of Vitacost.com;

FoodScience Corporation (Food Science of Vermont & DaVinci Labs);

Biopower Nutrition;

Thorne Research Inc.;

NBTY, Inc. (Puritan’s Pride);

Olympian Labs, Inc. (Prescribed Choice);

Now Foods;

Nature’s Sunshine Products, Inc.;

RHG & Company Inc. (Vital Nutrients);

The Natural Healing Room & End Time Essentials; and

Shine Supplements

The Office of the Attorney General has not sent a letter to Shine Supplements because the company could not be located through conventional means and is not registered with the Secretary of State to do business in New York.

Nature’s Way has also represented that it will refund the suggested retail price to any New York resident who purchased the company’s devil’s claw supplements between January 1, 2012 and the present and, within three months of the date of the letter, submits a sworn complaint to OAG using the form linked here. Refunds will be available one per household, with total refunds not to exceed New York sales of devil’s claw during the period.

In February 2015, Attorney General Schneiderman directed four major retailers—GNC, Walmart, Target, and Walgreens—to halt the sale of certain herbal supplements following DNA barcode tests that failed to detect plant materials listed on the labels of the majority of products tested and also detected DNA associated with ingredients or contaminants not listed on the label.

 

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