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Illinois Pharmaceutical Manufacturer Sued for Injuries to Kentucky Resident
Date:5/14/2008

hemselves, to ensure that these materials are acceptable for use." Moreover, the methods employed to test Heparin Sodium United States Pharmacopoeia (USP) had not been verified to ensure suitability under actual conditions of use and the equipment used to manufacture the product was "unsuitable" for its intended use.

China's Ministry of Commerce is now requiring local Heparin makers to increase testing of raw materials, improve post-sale tracking and ensure that their raw material comes from registered suppliers. This requirement follows U.S. Congressional inquiries into the FDA's overseas inspection process.

The House Oversight and Investigations Subcommittee held a hearing on April 15th of this year regarding the distribution of contaminated Heparin. A follow-up hearing took place on April 22nd at which time the committee asked FDA Commissioner Andrew von Eschenbach how the agency will address concerns regarding its efforts to inspect foreign drug facilities.

Mr. Banks is seeking judgment against all defendants for compensatory and punitive damages arising from the personal injuries that he suffered from the use of a pharmaceutical drug commonly known as Heparin.

Nolan Law Group is a Chicago-based personal injury law firm concentrating in aviation accidents, construction accidents, brain injury litigation, medical malpractice, premises liability, product liability, and trucking accidents.


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