Products Liability Lawyer in Illinois

Mislabeled Food Appears In Area Markets

A Colorado food processing company which failed to include peanuts in an on-label ingredient list blamed the incident on an “inadvertent packaging error.” The mistake could lead to severe, and possibly fatal, allergic reactions in millions of people.
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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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FDA Safety Alert Reveals Growing Number of Surgical Complications Involving Transvaginal Mesh

Transvaginal mesh is a medical device used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI). It is a permanent implant designed to strengthen a weakened vaginal wall in the instance of POP or to reinforce the urethra to treat SUI. In 2011, the FDA issued a follow-up of its health notification from three years previous, which alerted people to the complications linked to transvaginal mesh when treating either of these medical conditions.
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Risk of Blood Clotting with Birth Control Still an Issue

Thrombosis, or blood clots as they are colloquially known, tend to manifest naturally in men more than women. Women, however, are at risk for blood clots primarily because of pregnancy, birth control, and other hormonal therapies men do not generally take, according to StopTheClot.org.
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Invasive Procedure Equipment Causes Big Problems When Contaminated

With cancer rates at an all-time high and cancer remaining a leading cause of death in the United States, the word biopsy has become a household term.  A biopsy, according to WebMD, is the examination of a contaminated tissue that was removed from the body to determine what disease—or to what extent the disease is present—is afflicting a patient. A patient will undergo a biopsy if he or she has abnormal test results or if a medical practitioner suspects that it could identify an unidentified condition.
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Stryker and DePuy Artificial Hip Device Recalls Lead to Litigation

Metal-on-metal hips were first marketed as providing a greater range of motion and longer lasting use for patients. However, due to poor design and performance of certain artificial hips, failure rates have rapidly increased. Medical device manufacturers Stryker and DuPuy both created and promoted products that did not undergo proper testing. As a result, many have suffered.
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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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A Recall Issued For Yaz Was Not Publicized

Sometimes prominent drugs are recalled and no one knows about it. This was the case with a 2010 Food and Drug Administration (FDA) recall of the birth control Yaz, a contraceptive approved by the FDA for use among women as young as 14 years old. Yaz and Beyaz—a similar FDA-approved medication made by the same manufacturer, Berlex, Inc.—hit the market when it was approved in 2006, according to Drugs.com.
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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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  • Newland & Newland LLP, Attorneys, Arlington Heights, IL
  • Lawyer.com