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The New York Times has reported that a Johnson & Johnson/DePuy hip implant that was sold overseas, was rejected by the FDA in 2009.

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The implant was new hip resurfacing implant. Unlike traditional hip implants, in which the ball portion of thigh bone or femur is removed and a replacement stem and ball are implanted, this particular implant left the femur largely intact and placed a ball shaped cap over the existing femoral head. Most importantly for U.S. medical consumers, the same pelvic (or ace tabular) cup portion of the implants, was used in both the ASR resurfacing system and the ASR system which was approved and sold in the U.S. That ASR implant was eventually the subject of a recall in August 2010–a full year after the FDA had rejected the sister-product.

Both systems are so-called metal-on-metal hip implants because they involve a metal ball and a metal socket. The apparent problem with the implants is that the design of the metal sockets are such that the friction between the two components creates metal debris which reacts in many patients and causes infection-like responses, destroying bone, muscle, ligament and soft-tissues, leading to pain and dislocations of the hips. The metal can also seep into the blood and, in effect, cause a type of metal blood poisoning. The only way to stop the effects is to remove the metal cup and replace it with a traditional plastic lined cup.

The DePuy ASR implants are the subjects of thousands of lawsuits around the country. Most have been consolidated into a multi-district litigation based in the U.S. District Court for the Northern District of Ohio. However, many cases remaining pending in state courts throughout the U.S.

In related litigation, another DePuy metal-on-metal hip implant, the Pinnacle, has also seen cases consolidated in a multi-district litigation, this one in the Northern District of Texas. Generally, the same metal debris problems are occurring with the DePuy Pinnacle implants as occurred with the ASR implants.

For more information on the DePuy ASR Hip Implants, see my previous posts listed below. If you or a loved one have a DePuy ASR or DePuy Pinnacle implant, or suspect you have any metal-on-metal implant, call our offices immediately at 1-800-557-8176.

DePuy ASR Hip Implants Recalled

Hip Implants Withdrawn From Market

Metal on Metal Hip Components Linked to Early Failures

The New York Times has a recent article on The High Cost of Failing Artificial Hips that does a good job of outlining the the cost related to the seemingly epidemic failure of the metal-on-metal hip implants from DePuy and others. If you’ve had a hip replacement in the last 10 years, I would recommend that you read it here.

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If you have a DePuy ASR or Pinnacle metal-on-metal hip implant, I would strongly urge you to contact me to discuss your rights. Even if you are not currently experiencing problems with your hip replacement, you should be aware of the pending litigation and what you should do.

To be clear, there is no class action currently pending for these implants and I don’t anticipate that there will be. What is in place is called a Multi-District Litigation that has some of the characteristics of a class action, but differs in many ways. The most important difference is this: If you don’t file a lawsuit, your interests will not be protected and you will not receive a settlement. In the typical class-action anyone who can be identified as having received the defective product will receive notice of a settlement. That is not true in a Multi-District Litigation.

If you have had a DePuy ASR or Pinnicle, a Zimmer Duron or any other metal-on-metal implant, please contact me immediately at 1-800-557-8176 or see my website at www.stlmedicalmalpractice.com.

Medtronic medication pumps are widely used to deliver pain medication, anti-spasm medication and other prescriptions directly into the spinal cord. And the FDA has determined that these pumps can cause serious harm. The FDA has issued a Class 1 recall.

The SynchroMed II implantable pumps, models 8637-20 and 8637-40 are the subject of the recall which has been reported here. A Class 1 recall means that these pumps have a reasonable probability of causing serious adverse health consequences or death. The pumps are failing, apparently due to a defective design relating to the battery.

These pumps are surgically implanted under the skin with delivery tubes placed to the point of delivery. Medtronic is not recommending that the pumps be removed and replaced at this point, says MedPage Today.

If you or a loved one has experienced a failure related to one of these pain pumps, or if you have one of these pumps implanted, you should contact our office to discuss your legal rights. Contact us at 314-721-8833 or at www.stlmedicalmalpractice.com.