Patients filing hip replacement lawsuits have reported experiencing severe pain, swelling and difficulty walking caused by the Biomet M2a Magnum metal hip implants. Despite reports of complications, the U.S. Food and Drug Administration (FDA) has not issued a Biomet M2a Magnum recall.
Patients may be eligible to file a hip replacement lawsuit against Biomet Inc. if they experienced complications including:
- Fretting and corrosion
- Loosening of the hip implant
- Meal Poisoning
- Bone deterioration
- Hip implant dislocation
Many patients that have experienced complications from Biomet M2a Magnum hip implant failure have had to undergo hip revision surgery.
If you were implanted with a defective Biomet hip replacement system and experienced hip implant loosening, metallosis, fractures or other side effects that required corrective surgery, contact the hip replacement lawyers at Hissey Kientz, LLP to learn more about your legal rights. You can reach us by calling toll free at 1-866-275-4454, or by filling out a free case evaluation form.