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
Failed Medical Devices in the News: In 2007, Mr. Loren Kransky had an ASR hip prosthetic manufactured by DePuy Inc., a division of Johnson & Johnson, implanted into his right hip. He was told it was designed to last his lifetime, but it had to be removed four years later because design defects in the […]read more
The Cartwright Law Firm is issuing this Health Alert related to potentially faulty Medical Devices: Johnson & Johnson, already subjected to thousands of lawsuits following the 2010 recall of their ASR all-metal hip implants the company sold world-wide, has now recalled a second type of metal hip component it says was sold only outside of […]read more
The Cartwright Law Firm is issuing this urgent consumer alert regarding a contraceptive device known as the Mirena IUD. The device, manufactured by Bayer HealthCare Pharmaceuticals, Inc. and is used by more than 2 million women in the United States, was originally approved by the FDA in 2000 for contraception, and later as a treatment […]read more
Going in for surgery is almost always fraught with anxiety and fear. Few people, though, would ever think that the risks of surgery included the possibility of their bones catching on fire. Sadly, a defective medical product has made this a real possibility. Earlier this summer, the U.S. Food and Drug Administration asked Johnson & […]read more
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Robert E. Cartwright Jr.
Founder and Managing Partner
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