SETTLEMENTS COULD COST J&J AND ZIMMER $5 BILL

Forbes recently reported that the settlements related to the failing all-metal hip implants, which were implanted in nearly 500,000 patients, could reach close to $5 billion. Forbe's settlement estimate is based upon the assumption that, "the average cost to settle each all-metal hip replacement claim will be $169,000 [and] that the manufacturers will end up settling 30,000 claims."

OVER $80 MILLION PAID BY DEPUY AD ALLEGED KICKBACKS TO DOCTORS

DePuy Orthopedics has reportedly paid doctors and surgeons over $80 million in kickbacks for promoting DePuy devices. DePuy discloses doctor payments on the DePuy website and claims the payments are for consulting, research, or royalty payments. In 2007, the U.S. Department of Justice filed a criminal complaint against DePuy, alleging improper kickbacks made to doctors for promoting DePuy products. DePuy paid a substantial fine and agreed to pay physicians only for appropriate and legitimate services.
 

UPDATE: DePuy Hip Lawsuits Transferred to Northern District of Ohio for National Coordination

December 3, 2010: A seven-judge Judicial Panel on MultiDistrict Litigation today transferred the Depuy Hip Replacement Litigation to Judge David A. Katz of the Northern District of Ohio. As you know, the Litigation involves the recall of ASR Hip Implant Devices manufactured by Depuy Orthopedics Inc., a subsidiary of Johnson & Johnson. The hip devices were recalled after a National Joint Registry revealed that one in every eight people with these hip devices required a follow-up revision surgery. Close to 93,000 people have received the Depuy hip prosthesis.

Following the August 2010 hip recall, our office filed the first lawsuit in the United States. Recognizing the need to expedite this large case involving thousands of injured parties, our offices initiated the Motion to Transfer and coordinate the Depuy hip cases to streamline the process to the benefit of our clients. The granting of our Motion is a very significant and positive development that we are pleased to share with you.

We expect the transferee judge will very soon set a hearing for an initial status conference in the coordinated action.

 
Did you know that every year there are 200,000 to 300,000 U.S. citizens (primarily over the age of 60) who undergo hip replacement surgery? Usually, the people who decide to undergo the operation have been dealing with severe joint pain for years. This chronic pain can destroy a person's way of life by preventing them from enjoying what they used to enjoy most – morning walks with their spouse, playing in the backyard with their grandchildren, fishing, golfing, etc.

Although surgery is difficult, many times it is the only option. Hopefully, after the 1 ½ - 3 hr surgery, 5-10 days in the hospital after the operation, and up to ten weeks of intense physical therapy and rehabilitation, the patient may be able to walk again without pain. Patients have enough to worry about between the surgery, recovery, and possible long-term and short-term risks associated with the operation (such as blood clots, infections, dislocation of the prosthesis, change of leg length, etc.), to worry about another complicated surgery afterwards if the hip replacement doesn't properly take or deteriorates.

Unfortunately, close to 93,000 individuals who have received a hip prosthesis from DePuy Orthopedics Inc., a subsidiary of Johnson & Johnson, may be in need of revision surgery. Two of DePuy's orthopedic products, the ASR Hip Resurfacing System and the ASR XL Acetabular System, were recalled on August 26, 2010, after data from the National Joint Registry revealed that one in every eight people with these systems required a follow-up revision surgery.

If you or a loved one has received a hip implant recently, or within the last 5 years, and have experienced pain, swelling, or problems walking, you may want to consult your doctor to verify the prosthesis used.

Symptoms that indicate a need for a revision surgery include:

  • Loosening of the implant, when it does not stay in its proper position against the bone
  • Fracture of the bone surrounding the implant or
  • Dislocation of the implant, when the two adjoining parts are no longer correctly aligned

DePuy implants consist of ball and socket components made of metal that rub against one another as the joint functions  These implants, also known as metal-on-metal implants, often wear down over time, leaving small traces of metal within the blood, bone, and muscle tissue. While these traces are often too small to detect, thousands of people have reacted to these particles which can cause swelling, pain, and even permanent muscle, bone, and nerve damage.

If you have felt any of these symptoms, you should contact the surgeon who performed your hip operation. He or she should have a record of which prosthesis was used, and may take blood tests, x-rays, an ultrasound or an MRI to determine if you are in need of a follow-up operation. If you have received one of the recalled products but have not felt any symptoms or pain, you should still follow up with your doctor for the first 5 years after surgery, to ensure that the replacement continues to function properly.

If you do not know the surgeon who performed the surgery or the device that was used, contact the hospital where the surgery took place. The hospital representatives should have a medical record of the surgery and prosthesis.

This is the 11th recall of Johnson & Johnson's since September 2009. If you are one of the 93,000 patients who have received a recalled DePuy product, you should seek medical counsel immediately.  In addition, you may wish to pursue compensation for any medical expenses, pain or suffering consequently incurred. Take charge of your health and don't let years go by before you receive the medical attention you deserve.


DePuy implants consist of ball and socket components made of metal that rub against one another as the joint functions  These implants, also known as metal-on-metal implants, often wear down over time, leaving small traces of metal within the blood, bone, and muscle tissue. While these traces are often too small to detect, thousands of people have reacted to these particles which can cause swelling, pain, and even permanent muscle, bone, and nerve damage.

If you have felt any of these symptoms, you should contact the surgeon who performed your hip operation. He or she should have a record of which prosthesis was used, and may take blood tests, x-rays, an ultrasound or an MRI to determine if you are in need of a follow-up operation. If you have received one of the recalled products but have not felt any symptoms or pain, you should still follow up with your doctor for the first 5 years after surgery, to ensure that the replacement continues to function properly.

If you do not know the surgeon who performed the surgery or the device that was used, contact the hospital where the surgery took place. The hospital representatives should have a medical record of the surgery and prosthesis.

This is the 11th recall of Johnson & Johnson's since September 2009. If you are one of the 93,000 patients who have received a recalled DePuy product, you should seek medical counsel immediately.  In addition, you may wish to pursue compensation for any medical expenses, pain or suffering consequently incurred. Take charge of your health and don't let years go by before you receive the medical attention you deserve.

 
Free Case Review
If you or a loved one received a recalled hip device please feel free to call our case coordinator Jessica at
1-866-875-2262 or complete our free claim form below and we will answer your questions and assist you in this process.
 

 

 

 

 

 

 

 

 

 



 



 

 
  
 
 
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