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Case: Guidant Ancure Device Result: Confidential Settlements On June 23, 2003, Ken Moll's law firm filed the first worldwide class action lawsuit against Endovascular Technologies, Inc., a Guidant company, for serious injuries and death of users of its defective Ancure Endograft Systems, devices used to treat abdominal aortic aneurisms

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The new rule reiterates that a product made or derived from tobacco will be subject to FDAs medical product (i.e., drug) authority, and not its tobacco authority, if it is intended (a) for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment or prevention of disease, including use in the cure or treatment of nicotine addiction (e.g., smoking cessation), relapse prevention, or relief of nicotine withdrawal symptoms