DePuy Orthopedics Inc., a subsidiary of Johnson & Johnson announced the recall of its products, ASR XL System Acetabular hip and ASR System coatings have been numerous reports of defects and damage caused by these devices.
The reason for the recall on hip replacement is also a large number of systems reviews of the hip. DePuy statistics showed that 12% of patients who received the device ASR resurfacing and 13% of patients who have their roots in hip surgery must complete the surgery or what they call the review section.
Approximately 93, 000 people have been planted with a defective hip. These people are at risk or suffering from serious injuries caused by equipment failure.
Most patients complain of persistent pain, swelling, and even dislocation of the implant. These injuries cause suffering and discomfort and the only permanent solution to this is to have another surgery to replace the defective hip replacement with new ones. This revision surgery means an additional expense and painful procedures.
ASR hip was manufactured and distributed from July 2003, which means that all patients who underwent hip surgery or after that date may be subject to this recall on hip replacement. If you are having surgery at this time, it is best to contact your doctor and ask if the replacement system that was part of the device to replace the defective hip DePuy, but if I had the hip before date, you can rest assured that no affected by this recall.
If you are sure that this seems to remember that it is best to contact the lawyers of the hip recall immediately. They are professionals when it comes to this subject. They can say what to do and could also be in court against the company that you deserve to get compensation after the absence of a hip system has caused.
Immediate action is needed if you are affected by this recall on hip replacement, because the law allows only a certain period for patients who have been victims of these systems defective hip to intervene. There is no reason to delay.
The reason for the recall on hip replacement is also a large number of systems reviews of the hip. DePuy statistics showed that 12% of patients who received the device ASR resurfacing and 13% of patients who have their roots in hip surgery must complete the surgery or what they call the review section.
Approximately 93, 000 people have been planted with a defective hip. These people are at risk or suffering from serious injuries caused by equipment failure.
Most patients complain of persistent pain, swelling, and even dislocation of the implant. These injuries cause suffering and discomfort and the only permanent solution to this is to have another surgery to replace the defective hip replacement with new ones. This revision surgery means an additional expense and painful procedures.
ASR hip was manufactured and distributed from July 2003, which means that all patients who underwent hip surgery or after that date may be subject to this recall on hip replacement. If you are having surgery at this time, it is best to contact your doctor and ask if the replacement system that was part of the device to replace the defective hip DePuy, but if I had the hip before date, you can rest assured that no affected by this recall.
If you are sure that this seems to remember that it is best to contact the lawyers of the hip recall immediately. They are professionals when it comes to this subject. They can say what to do and could also be in court against the company that you deserve to get compensation after the absence of a hip system has caused.
Immediate action is needed if you are affected by this recall on hip replacement, because the law allows only a certain period for patients who have been victims of these systems defective hip to intervene. There is no reason to delay.
About the Author:
Learn more about recall on hip replacement. Stop by Jeffry Hilton's site where you can find out all about recalled hip replacement and what it can do for you.
No comments:
Post a Comment