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Guidant Pacemakers
FDA Study Shows Defibrillator Malfunctions are on the Rise
Sep 26, 2005 | www.newsinferno.com
The U.S. Food and Drug Administration (FDA) has released its review of implantable cardioverter defibrillator (ICD) and pacemaker (PM) malfunctions...
Guidant Issues Fifth Product Recall This Year
Sep 23, 2005 | www.Newsinferno.com
Guidant Corp. issued recalls Thursday for some of its best-selling pacemakers. Citing problems with the Insignia and Nexus families of...
Health Canada Advises Canadians About Risks Associated With Guidant Pacemakers
Aug 4, 2005 | Health Canada
Health Canada is advising Canadians who have implanted PULSAR MAX, PULSAR, DISCOVERY, MERIDIAN, PULSAR MAX II, DISCOVERY II, and CONTAK TR...
Guidant May Face Senate Scrutiny
Jul 31, 2005 | Star Tribune
At first blush, it might seem a bit unusual that the chairman of the Senate Finance Committee has taken a sudden interest in a series of heart device...
Parker & Waichman, LLP Investigating Claims of Victims Injured by Recently Recalled Guidant Pacemakers
Jul 22, 2005 | PrimeZone
Parker & Waichman, LLP (www.yourlawyer.com) announces that it has commenced an investigation into defective pacemakers manufactured by Guidant...
Guidant Issues Warning for 28,000 Pacemakers
Jul 18, 2005 | AP
Guidant Corp. on Monday warned physicians that replacements might be needed for nine pacemaker models made between 1997 and 2000, of which some...
FDA Announces Guidant’s Class I Pacemaker Recall
Jun 22, 2005 | ww.fda.gov
The U.S. Food and Drug Administration (FDA) is notifying health care providers and patients that Guidant Corporation is voluntarily recalling certain...
Guidant Pacemakers
