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The Chicago Tribune has reported that Des Moines, Iowa attorney Guy Cook has reached confidential settlements on behalf of 3 persons injured by a defective lounge chair sold by K-Mart under the Martha Stewart brand. The full story can be found here.

The chairs were defectively designed. The design allows the legs to snap forward and creates a guillotine effect. Numerous persons have experienced complete or partial amputations of fingers or fingertips. K-mart and Martha Stewart continued to sell the chairs for a period of time even after the first lawsuits were filed.

If you’ve been injured by a defective product, please contact the offices of HendricksonLaw.com to discuss your rights.

DePuy, a division of Johnson & Johnson, has issued a recall on its ASR hip replacement components, including the ASR Hip Resurfacing System and the ASR XL Acetabular System. You can read about the recall here.
The DePuy ASR components are known as metal-on-metal components. Rather than using a poly-vinyl, ceramic or other material pelvic cup surface, the DePuy, like many other manufacturers, designed the ASR system to utilize a metal ball head and metal pelvic cup. The result is apparently is a disaster.
By some reports, more than 13% of these implants are failing within five years. The average him implant lasts 15-20 years before it wears out and needs to be revised. The highest rate of failure is in the smaller ASR implant sizes, 50mm and less, the most common sizes implanted in women.
If you have an ASR hip implant that has been revised due to early loosening or other problems, please contact the office of Todd N. Hendrickson immediately. Our office is aggressively investigating these cases and can help you. It is important that you be represented by an experienced medical malpractice and medical product liability lawyer, as DePuy will attempt to defend these cases by claiming that surgeon error in implantation. Don’t trust your case to a so-called “mass tort” law firm that doesn’t prosecute medical malpractice cases.
Contact our office today, by clicking on this link.

Byetta, a drug used to treat Type II diabetis, is suspected of causing hemorrhagic or necrotizing pancreatitis in numerous patients. As a result, the FDA has issued an alert. Byetta is given by injection. If you are taking Byetta, you should immediately discuss this information with your physician. Information for your doctor can be found here.If you suspect that you or a loved one has been injured as a result of using Byetta or any other drug or as a result of medical malpractice, please contact Todd N. Hendrickson.