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Johnson & Johnson's DePuy Orthopedics, Inc. has Recalled it's ASR XL Acetabular System
DePuy Orthopedics, Inc., the orthopedic division of Johnson and Johnson, has issued a recall of two artificial hip implant components. This type of metal on metal hip implants have ball and socket joints that are made from metals such as cobalt and chromium. As the metal components rub against each other in a typical joint fashion, they shed metallic particles into the patient's body, causing inflammation, pain, possible death of tissue in the hip joint, and even loss of surrounding bone.
DePuy's August 24, 2010 letter to clinicians stated:
"Reasons for revision ... include component loosening, component malalignment, infection, fracture of the bone, dislocation, metal sensitivity and pain."
It further states that a "number of patients may develop progressive soft tissue reactions to metal wear debris. The debris can cause soft tissue damage which may compromise the results of the revision surgery."
See full August 24, 2010 letter from DePuy Orthopedics, Inc.
DePuy has sold approximately 93,000 of this type of artificial hip implant. It is unknown how many of the patients, in which these hips were implanted, will require additional surgery to replace them.

If you have suffered a failed hip implant, contact us for a free consultation.

Avandia, otherwise known as Rosiglitazone, is an anti-diabetic drug which has been shown to increase the risk for heart attack by as much as 43% and increase the risk of stroke by more than 27%. It is also linked to an increase of risk for congestive heart failure and other cardiovascular issues, loss of bone strength, fractures, osteoporosis, and liver failure.

If you have taken Avandia, and you feel it has caused you to suffer a medical problem, please contact us for a free consultation.

Meridia, also known as Sibutramine, is a diet drug which raises blood pressure and heart rate, increasing the risk for heart attacks and strokes. According to the drug's manufacturer, Abbott Laboratories, they are voluntarily withdrawing Meridia from the market due to pressure by the Food and Drug Administration.

If you have taken Meridia, and you feel it has caused you to suffer a medical problem, please contact us for a free consultation.
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Dell Class Action Lawsuit Norman, et al., v. Dell, Inc. et al. Case No. 07-CV-6028-TC U.S. District Court for the District of Oregon

Families of Oregon's Adopted Foster children to Receive Compensation for Adoption Assistance Payment Cuts in 2003

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