Several hip replacement patients have filed lawsuits against the manufacturer of the Biomet M2a Magnum hip implant, claiming that the device is defectively designed and prone to early device failure. If you or someone you love was injured due to the Biomet M2a Magnum hip implant, consider seeking legal counsel from a Biomet hip recall lawyer to learn more about your rights and determine if you are eligible to hold the manufacturer responsible for compensation for your condition.
Lawsuits involving the Biomet M2a Magnum implant claim that friction between the device’s metal cup and ball can generate large amounts of cobalt and chromium ions. Plaintiffs also claim that the metal debris shed from the implants can accumulate to dangerous levels in the bloodstream and surrounding tissues, leading to several serious complications, including:
- Tissue death
- Metallosis
- Formation of pseudotumors
- Disintegration of bone
- Long-term or permanent disability
- Chronic pain requiring revision procedures
Since February 2011, the U.S. Food and Drug Administration has been reviewing metal-on-metal hip implant devices including the Biomet M2a Magnum. On January 17, 2013, the agency submitted a Safety Communication in which it reported that the metal ions shed from the implants may cause damage to soft tissues or bones surrounding the joint and implant.
As a result, patients in California and across the U.S. may experience device failure, implant loosening, pain and the need for revision surgery. The metal ions may also travel through the bloodstream, where they may potentially cause illnesses or symptoms elsewhere in the body. The FDA is now advising that metal-on-metal hip recipients be considered for metal ion testing if they begin to suffer from symptoms of a failing device.
Although the FDA is actively investigating all metal-on-metal hip implants, plaintiffs argue that Biomet hip implants were never adequately tested. As is the case with most of the other metal-on-metal devices on the market, the M2a Magnum was approved via the FDA’s 510(k) clearance program without human testing as it had been demonstrated to be similar in design and function to a device already on the market.
This approval process has recently become controversial, as critics and those working with a Biomet hip recall lawyer allege it allows potentially dangerous devices to become available without proper testing. The FDA has proposed a new rule that would make all metal hip replacement devices ineligible for the program. However, those who have been injured and who are working with a Biomet hip recall lawyer claim that, while this is a positive step forward, it does little to help those who have already been injured.
If you have a claim, you may be able to work with a Biomet hip recall lawyer in California to recover damages for your injury. Permanent disability costs, pain and suffering, medical expenses, loss of past and future income and certain out-of-pocket expenses could potentially be recovered.
Contact a California Biomet Hip Recall Lawyer Today
If you or someone you love sustained an injury due to an allegedly defective Biomet metal-on-metal hip replacement device in California, you may be able to seek compensation for lost wages, pain and suffering and medical expenses. Contact Attorney Group for California to receive a free case evaluation and determine whether you have a claim. We can answer your questions and connect you with an affiliated Biomet hip recall lawyer in California who can assist you throughout the legal process.
Source:
http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm335775.htm
