Biomet M2a Hip Replacement Lawsuits and Settlements
Biomet Metal on Metal Hip Replacement Lawsuits
The Biomet M2a-38 and the M2a-Magnum are metal on metal hip implants with a history of serious complications. Patients across the United States have filed lawsuits demanding Biomet take responsibility for making and selling defective hips.
Patients are suffering from metal poisoning, metallosis, ALVAL, heart damage, pseudotumors, dead muscle and bones, and a very long list of other medical problems. Many are forced to get a brutal revision surgery to remove the Biomet metal on metal hip and replace it with another type of implant.
mctlaw is one of the few law firms in the country still reviewing medical records and filing lawsuits for people hurt by this specific hip.
What is Wrong with the Biomet M2a Magnum Hips?
The Biomet M2a Magnum hips were poorly designed from the start. The idea behind metal on metal hips is that the body’s own fluids would provide enough lubrication between the cup and the ball of the hip replacement. Instead, the cobalt and chromium metal surfaces of the hip and the cup rub and grind together, releasing microscopic metal debris into the hip cavity. That metal can destroy the muscle, bone, and other tissue surrounding the hip. The metal dust is also small enough to enter the bloodstream and cause metal poisoning throughout the body.
Biomet and it’s sales representatives convinced many surgeons across the US about the promise of the Magnum M2a metal on metal hip implants. Unfortunately, and unknown to most people (including surgeons), more than 95% of medical devices like the Biomet M2a Magnum hips make it into a patient’s body without a single test for safety or effectiveness. Basically, the majority of the patient population became live test subjects without even knowing it. When that happens, patients like our metal on metal hip clients have horrifying medical outcomes.
Biomet has not taken responsibility for making and selling a hip that is devastating people’s health and their lives. The problem of sales before safety is so bad that Biomet warned surgeons about these hips in Australia and Europe, but did not warn American surgeons at the same time, and kept on selling the hips in the United States.
Metal on Metal Hip Replacement Cases Across the United States
Click on each state to view the number of cases.
Find Out Now if You Have a Biomet HIp LAWSUIT
Your case review is free. There is a statute of limitations, so don’t wait.
Biomet Issues “Hazard Alert” for M2a Hip Implants in Australia
Biomet stopped supply and sales of its M2a hip replacement components and canceled them from the Australian Register of Therapeutic Goods (ARTG).
In February 2015, Biomet issued a “hazard alert” for these metal on metal (MoM) components because the Australian Orthopaedic Association has data showing a much higher than expected revision rate.
Zimmer Biomet has not issued similar warnings or recalls for the identical metal on metal hip parts sold in the United States.
Biomet Sends Warning Letters to Surgeons in Europe
In April 2016 the company sent letters to surgeons in Europe admitting the M2a hip had a higher than expected revision rate. The warning is called a Field Safety Corrective Action and is based on data collected by the National Joint Registry for England, Wales and Northern Ireland.
Biomet did not send a similar warning to U.S. surgeons.
Metal Debris from Biomet M2a Magnum Hips Linked to These Severe Health Issues:
5 Steps to Take Now if you Have a Biomet M2a Metal on Metal Hip
See Your Doctor for a Follow-Up Exam – Even if you Don’t Have Symptoms
Ask your surgeon if you should get a MARS MRI or CAT scan of your hip. These tests look for pseudotumors or adverse reaction to metal debris ARMD. However, even if you don’t have any symptoms, you still may have problems related to your metal hip. Doctors may not know to look for a MoM hip problem if you don’t have symptoms.
Ask your doctor to test your blood for high levels of cobalt or chromium. Friction between the metal cup and ball rubbing together can cause metal particles to rub off and enter your bloodstream. This is sometimes a sign of metallosis, which can cause devastating medical conditions.
Hire an Attorney BEFORE Revision Surgery, if Possible
It is extremely important to preserve removed Biomet M2A and Magnum metal-on-metal hip replacements for evidence.
It’s important to preserve pathology specimens. These document the amount and effect of the metal debris generated by the metal on metal hip replacement.
Maglio Christopher & Toale Law Firm is a leader in obtaining and preserving such evidence. We can help your surgeon retrieve and store the device and specimens.
If you already had revision surgery, don’t worry. Our attorneys will likely still be able to recover evidence from your procedure. That’s why we work as a team with your orthopedic surgeon.
Get a Copy of Your Hip Implant Records
Your hip implant record is a key piece of evidence in your case. Ask your surgeon to give you a copy of the implant record and the operative notes. Click here to see a replica of an implant record.
The implant record is a piece of paper with stickers on it. These labeled stickers are removed from the hip implant packaging before surgery. The stickers will show what brand of hip device you have and should also include a barcode or serial numbers. Implant records also typically include the patient’s name, surgery date, and the hospital where the replacement surgery was performed.
What if I Have Trouble Getting These Medical Records?
These are your personal medical records and you have a right to a copy of them. The Biomet hip replacement attorneys at Maglio Christopher & Toale Law Firm can help you collect and review these medical records in order to preserve evidence for a claim. Please contact us immediately to begin a case evaluation. You can call us at (888) 952-5242 or fill out our form below.
Report Your Problem to the FDA
There is a way to help bring these issues to the attention of the FDA, but there is: Report your adverse metal on metal hip experience to the FDA by filling out a MedWatch form.
Hip manufacturers are required to report all hip failures to the FDA. However, they often find loopholes to keep this data hidden. If the FDA doesn’t have accurate reporting of patients experiencing serious complications, then neither does your surgeon. Doctors rely on FDA data to diagnose problems and know when a specific type of hip implant experiences issues.
Don’t let the hip implant makers brush your information under the rug. Most people don’t know that you can self-report problems, but the FDA needs to hear from you. Empower yourself against these huge corporations that put profits above your health. It’s simple to fill out the form. More importantly, it’s a good way to make your voice heard.
Sign the Petition Demanding the FDA Recall the Biomet Magnum & M2a Hips
Demand the FDA do its job and recall the Biomet Magnum and M2a-38 metal on metal hip replacements. Why? Because these hip replacements are causing heavy metal poisoning resulting in tissue destruction, pseudotumors, bone deterioration, and heart failure. Patients and surgeons have been left in the dark.
Zimmer-Biomet has known of these problems for years. The company even recalled these hip replacements in other parts of the world, but not here. Zimmer-Biomet has failed to warn patients and surgeons in the United States of the heavy metal poisoning. Demand the FDA do its job and recall this dangerous product. Patients and surgeons must be warned of the risks.