products liability

Are all supplements tainted?

Nearly all of the herbal dietary supplements tested in a Congressional investigation contained trace amounts of lead and other contaminants, and some supplement sellers made illegal claims that their products can cure cancer and other diseases, investigators found. So begins an article in the New York Times on a Government Accounting Office report released May [...]

Orlistat and Hydroxycut: Similar health problems, but comparable FDA treatment?

This is a tale of two types of weight-loss products and how the Food and Drug Administration had different responses to similar problems with them. The separate, but not equivalent treatment raises questions about how the FDA operates.

As we enter our 5th year, a new look but the same mission for NutriSupLaw

If you have not visited the NutriSupLaw blog in a little while, you should. To celebrate the start of our fifth year, we gave the blog a makeover. Or as they say on the Web, a redesign. We think the new look does a better job of displaying blog entries and organizing our growing lists of resources, links and tags.

Sunscreen advertising war heats up

GUEST COLUMN by Judith L. Grubner, Esq., Arnstein & Lehr Partner and Intellectual Property Practice Group Leader Some of us remember when parents would chase their children out to play in the sun, with no protection other than play clothes.  Today, the Federal Trade Commission tells us overexposure to the sun’s invisible rays – ultraviolet [...]

Vitamin D at 5,000 IU: Too high, or just too soon?

Some dietary supplement companies are boosting their dosages now. The increases have implications not only for consumer health but for regulatory action. The agency might issue warning letters to companies selling Vitamin D products containing 2.5 times the current UL, telling those manufacturers that their products are potentially unsafe.

For Zicam’s maker, troubles do not end with recall

Manufacturers beware. Your regulatory problems may not be over when you pull a product from the store shelves. Matrixx Initiatives Inc. recalled its Zicam products on June 16 and three days later the Securities & Exchange Commission sent a letter of inquiry. The company said that it did not know what the regulatory agency wanted, [...]