Things About ASR Hip Recall That You Should Know

DePuy Orthopaedics has recalled the DePuy ASR (Articular Surface Replacement) Hip Resurfacing System and ASR XL Acetabular System total hip replacement following data showing that there are more people than expected who experienced debilitating pain or other serious side effects resulting from the hip implant devices.

A considerable number of these patients have since necessitated another hip replacement procedure that would correct problems correlated with the DePuy devices. Now, hundreds of lawsuits are piling up against the manufacturer in the aftermath of painful and debilitating side effects.

Research data gathered by the National Joint Registry of England and Wales showed that five years after the initial surgical implantation, there was 12 percent of those implanted with the ASR resurfacing device, and 13 percent of ASR total hip replacement recipients, needed a corrective hip replacement surgery to remedy the problems caused by the devices.

DePuy ASR products first came into the market in July 2003, and the DePuy ASR metal-on-metal hip replacement device is estimated to have been implanted in more than 13,000 patients internationally since its introduction. Before the recall, research studies took note of several painful and sometimes irreversible side effects linked to the DePuy hip system. It includes the following:

Loose ASR cupr
Allergic reaction to metallic debrisr
Pseudotumors (presence of soft tissue mass that forms resulting excess metallic debris reactions)
Cobalt or chromium poisoning

Moreover, a lot of doctors think that the DePuy ASR hip cup parts is too shallow, preventing its proper implantation which in turn leads to hip complications.

Upon its issuance of recall, DePuy admitted that it issued the recall because of the big number of patients requiring corrective surgery to remove the devices resulting from its failure.

Later, as the company became deeply embroiled in legal battles raised by patients who have had the procedures for the removal of the defective implants, problems with the device was denied by DePuy. The company stated that their withdrawal of the devices from distribution was merely based on the device’s waning popularity and the company’s shift to emerging hip-replacement technologies.

As a recipient of the ASR Hip Resurfacing System or the DePuy ASR XL Acetabular System, DePuy Orthopaedics or Johnson & Johnson might contact you regarding the recall of these devices. It is, however, pertinent to seek the experienced legal counsel before seeing a doctor or signing any paperwork supplied by the companies. It DePuy Pinnacle Hip Litigation Highlights Dangers of Hip Replacement Risks http://www.rotlaw.com/depuy-pinnacle/ might happen that you are being made to sign a waiver that will keep you from receiving any compensation for future medical expenses that may arise.

Although the companies may offer compensation, it may now be enough to cover some medical expenses, blood tests or diagnostic exams that may be required by doctors necessary in checking certain complications such as “metallosis,” or a serious allergic reaction to the presence of metal debris in the body. The compensation package may also not be enough to cover additional losses such as lost wages, loss of earning capacity or pain and suffering.