Defective Medical Device

Regulation of Defective Medical Devices

Every month the Food and Drug Administration (FDA) recalls several products and devices as unsafe for consumption. Many of these never make news, and very few of these ever make a big splash in the mainstream media. This makes determining whether or not you’ve been affected by a defective product or device difficult.
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Defective Medical Device Behind Veteran’s Death

Doctors stated that veteran Eddie Creed’s death last year was the result of throat cancer, but some journalistic investigations have revealed that there may be more to the story regarding a defective medical device. Creed had been using a medical device called Infusomat, a device which had actually been recalled a month before he started using it.
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Mirena IUD Parent Company Named in Lawsuit

An intrauterine device (IUD) is a commonly preferred method of birth control used by many women, suggested for use in women who have had at least one child. According to WebMD, “an IUD is a small, T-shaped plastic device that is wrapped in copper or contains hormones.” It is implanted into the uterus by a medical professional, and stays in place, releasing hormones on a schedule for up to five years.
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Negative Side Effects of Infuse Bone Graft Continue

Medtronic Inc. devised a bone graft device known as Infuse Bone Graft, which hit the market in 2011. As of mid-2013, the Infuse had been used in millions of surgeries across the nation, touted as a safer alternative to a bone graft after spinal surgery.
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Company Fined $2.2 Billion Over Defective Hip Implants

In an attempt to settle thousands of defective medical device lawsuits over its recalled hip implants, Johnson & Johnson subsidiary DePuy has agreed to pay at least $2.47 billion. Patients have told a judge while outlining an accord, however, that the final settlement may be worth more than $4 billion total. The global health care company recalled 93,000 defective ASR hip implants in 2010. Doctors and patients began complaining that the implants are weak and internal company documents have shown that 37 percent of the implants fail within 5 years.
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FDA Warns Stress Test Drugs may Cause Heart Attacks

The United States Food and Drug Administration (FDA) has announced that two chemicals that are used in heart stress tests can cause heart attacks and can also cause death. The chemicals, Adenoscan and Lexiscan, are both manufactured by Astellas Pharma US Inc.
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Surgical Mesh Implants for Hernia Repair may Cause Chronic Pain

A lot has been noted about the dangers of transvaginal mesh implants, most commonly used for pelvic organ prolapse repair and/or stress urinary incontinence, according to the U.S. Food and Drug Administration (FDA). Transvaginal mesh is only one type of surgical mesh used however—a device generally implanted to “repair weakened or damaged tissue.” Another common use for surgical mesh devices is for the repair of hernias.
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Report Defective Medical Device Complaints via MedWatcher App

If you have ever experienced painful side effects due to a defective medical device, drug or vaccination, you are not alone. Consumer Reports notes that “tens of millions of Americans live with medical devices implanted in their bodies,” including artificial joints, heart defibrillators and surgical mesh. And while Americans may assume that these devices have been tested for safety and effectiveness, Consumer Reports indicates that this is rarely the case.
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  • Newland & Newland LLP, Attorneys, Arlington Heights, IL