Hip Device Defects Call Out for Stryker Hip Recall
The manufacturer of devices for orthopedics gave the most recent information about Stryker hip replacement recall order for two hip components with the modular-neck and stem design due to the posing dangers of disintegration which can lead to painful tissue inflammation.
For the past few years up until now, a definite number of Stryker hip system designs are consequently being subjected to a series of product recall. Despite the previous recalls, FDA has still granted the released of the new Stryker metal-on-metal hip replacement device.
The recall order concerns all devices of Rejuvenate and ABG II Modular- neck and stem components. Stryker launched the recall after the post market study revealed the tendency of the hip device to easily fray and corrode. The adverse reports are also being supported by the Food and Drug Administration in the United States.
The addition of a detachable hip stem to the hip replacement device will mechanically allow more versatility for the surgeon to provide the appropriate hip device fitting according to the body of the patient. The two part hip component design is the company’s assurance of a long lasting artificial hip foundation. However, Stryker’s advertising was not affirmed by the post market evaluation.
The voluntary recall is also due to the many adverse effects recorded by the Stryker Company. The Stryker hip devices are allegedly causing painful sensation and swollen soft tissues along the hip joint area of the implant considering that these are not attributed by any other complications.
Further studies have also revealed the dangers of metal deposits in the body caused by the rubbing of two hip components that are both made out of metal. The accumulation of metal fragments can actually initiate other physiological complications such as bone fragmentation, cardiac arrest and metal poisoning.
The most common risk is the elevated level of metal deposition in the body. Damaged muscle tissue will gradually die from the exposure of chromium and cobalt metal compounds. Doctors have also observed the discoloration of the muscles during a secondary hip revised implant to repair the defective Stryker hip system.
Most of the critical side effects are disclosed to the surgeons and orthopedic specialists. However, it is not completely published in the public. After the recent Rejuvenate Modular and ABG II neck and stem recall last July 6, 2012, a number of patients now seek for defective device compensation claims. This has mounted to several Stryker lawsuits.
URL Reference: livestrong.com/article/207903-most-common-side-effects-after-hip-replacement-surgery/
For the past few years up until now, a definite number of Stryker hip system designs are consequently being subjected to a series of product recall. Despite the previous recalls, FDA has still granted the released of the new Stryker metal-on-metal hip replacement device.
The recall order concerns all devices of Rejuvenate and ABG II Modular- neck and stem components. Stryker launched the recall after the post market study revealed the tendency of the hip device to easily fray and corrode. The adverse reports are also being supported by the Food and Drug Administration in the United States.
The addition of a detachable hip stem to the hip replacement device will mechanically allow more versatility for the surgeon to provide the appropriate hip device fitting according to the body of the patient. The two part hip component design is the company’s assurance of a long lasting artificial hip foundation. However, Stryker’s advertising was not affirmed by the post market evaluation.
The voluntary recall is also due to the many adverse effects recorded by the Stryker Company. The Stryker hip devices are allegedly causing painful sensation and swollen soft tissues along the hip joint area of the implant considering that these are not attributed by any other complications.
Further studies have also revealed the dangers of metal deposits in the body caused by the rubbing of two hip components that are both made out of metal. The accumulation of metal fragments can actually initiate other physiological complications such as bone fragmentation, cardiac arrest and metal poisoning.
The most common risk is the elevated level of metal deposition in the body. Damaged muscle tissue will gradually die from the exposure of chromium and cobalt metal compounds. Doctors have also observed the discoloration of the muscles during a secondary hip revised implant to repair the defective Stryker hip system.
Most of the critical side effects are disclosed to the surgeons and orthopedic specialists. However, it is not completely published in the public. After the recent Rejuvenate Modular and ABG II neck and stem recall last July 6, 2012, a number of patients now seek for defective device compensation claims. This has mounted to several Stryker lawsuits.
URL Reference: livestrong.com/article/207903-most-common-side-effects-after-hip-replacement-surgery/