As a consumer alert on faulty medical devices, The Cartwright Law Firm wants to warn consumers who may have had a cardiac rhythm device implanted to be aware of the following issue: Medtronics, Inc. issued the following press release under urging from the FDA in response to what the FDA terms a Class 1 recall: […]read more
*An FDA Alert! – The FDA is warning the public that azithromycin (Zithromax or Zmax) can cause abnormal changes in the electrical activity of the heart that may lead to a potentially fatal irregular heart rhythm. Patients at particular risk for developing this condition include those with known risk factors such as existing QT interval […]read more
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Founder and Managing Partner
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