Published in Drug Law Weekly, August 25th, 2009
Minneapolis, Minnesota-based pharmaceutical company Medtronic, Inc. recalled its Sprint Fidelis
Defibrillator Leads, models 6930, 6931, 6948 and 6949 on October 15, 2007. According to the FDA the leads were recalled because of the potential for fracture which can result in the...
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Source: Drug Law Weekly (2009-08-25)
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