Illinois defective product attorney

Defective Wheelchair Lifts Sold Even After Recall

Defective medical devices are not limited to those implanted in a patient’s body. Patients who must use canes, wheelchairs, or other devices to get around are susceptible to a whole array of device warnings and risks that other Americans are not.
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Pain Pumps Can Necessitate Further Surgeries

Sometimes a medical device meant to provide relief for patients suffering and expedite healing causes more pain than relief. One of these devices is known as a pain pump, most commonly used in patients recovering from shoulder surgery after a serious shoulder injury.
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The Many Side Effects of SSRI Therapy

Many risks of anti-depressants are relatively well-known and publicized. One of the most common side effects of anti-depressants occurs when expectant mothers take them. Selective Serotonin Reuptake Inhibitor antidepressants (SSRIs) have a very high risk of resulting in birth defects in a newborn, reports the National Library of Medicine, part of the National Institute for Health (NIH).
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FDA Issues Largest-Ever Medical Product Recall in 2014

The U.S. Food and Drug Administration (FDA) issued its largest recall of medical products ever in 2014, according to the Regulatory Affairs Professional Society (RAPS). The recall, posted to the FDA’s website in August, was of 233 Class I products manufactured by Puerto Rico-based Customed.
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Lawsuits Brought Against Eli Lilly, Manufacturer of Cymbalta

Cymbalta is a multi-use prescription drug most commonly used as an anti-depressant. Despite several clinical trials during the approval process of Cymbalta that alleged Cymbalta caused depression in otherwise healthy patients, the U.S. Food and Drug Administration did not recall the drug for use as an anti-depressant, according to the New York Times.
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Lawsuits Brought Against Xarelto for Internal Bleeding

Xarelto is a blood thinner prescribed to patients at high risk of blood clots or strokes and is widely prescribed by the medical community. It can also be used to treat pulmonary embolism and can be used to reduce the risk of clotting in a person who has just undergone joint replacement surgery. According to the Xarelto website, more than 9 million people worldwide have been prescribed Xarelto for various reasons.
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Senators Call for Recall of Power Morcellators

In August, two U.S. senators began pressing the Food and Drug Administration (FDA) to take power morcellators off the American medical device market. According to the FDA, laparoscopic power morcellators are used to help remove tissue through small incision sites, and are most commonly used in hysterectomies or during the surgical removal of uterine fibroids (myomectomy).
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Guidant Case Reveals Problems with Defective Device Investigations

Finding out that you or a loved one has suffered injuries or requires additional procedures to correct problems from a defective medical device is frustrating. There are certain steps you need to take to protect yourself and to have the best chance of getting the company to recall or fix defective devices.
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  • Newland & Newland LLP, Attorneys, Arlington Heights, IL
  • Lawyer.com