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Ask a Heart Device Recall Lawyer, "Do I have a Case?" : Heart Device Recall Blog : November 2005
Guidant Corp. said it was served with subpoenas from U.S. Attorney's offices in Boston and Minneapolis seeking documents concerning pacemakers, defibrillators and related products. The subpoena from the Boston office is apparently part of an industrywide investigation. Two other medical device companies, St. Jude Medical and Medtronic Inc., said they also received subpoenas from that office. Indianapolis-based Guidant said the subpoena from the Minneapolis office relates to its Ventak Prizm and Contak Renewal defibrillators, which were among products hit by recall notices in the past several months. Jeff Swiatek, The Indianapolis Star, 10/26/2005
Health Canada: Important Safety information on certain St. Jude Medical implantable cardiac defibrillatorsNovember 16, 2005 07:36
Important Safety information on certain St. Jude Medical implantable cardiac defibrillators
Medtronic says SIGMA some pacemakers faultyNovember 30, 2005 05:59 edtronic Inc. said on Tuesday it is advising physicians of a potential problem in a small number of its Sigma pacemakers in which wires may separate from a circuit. The Minneapolis-based medical device maker said the overall incidence rate is "extremely low" and there have been no reports of patient injuries or deaths related to the issue. Yahoo reports Reuters News.
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