Cartwright - November 18, 2013 - Blog, FDA Alerts

Faulty Medical Devices Recall by Medtronics: FDA Issues Class 1 Status

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: […]

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Cartwright - March 13, 2013 - Blog, FDA Alerts

FDA Alert – Z-Max Antibiotic May Affect Heart Rythym Fatally

*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 […]

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Robert E. Cartwright Jr.
Founder and Managing Partner

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