Contact UsTwo Pershing Square 2300 Main Street, Suite 170 Kansas City MO 64108
Two Pershing Square
2300 Main Street, Suite 170
Kansas City, MO 64108
Telephone: (816) 221-6600
Toll Free: (877) 284-6600
Fax: (816) 221-6612
In 2007, Elizabeth Sones had surgery on her hip and received an implant with Biomet M2a Magnum components. Thereafter, she experienced pain and difficulties and it was determined that she had a condition consistent with a pseudotumor. The biomet magnum was revised as a result of failure of the device, leaving her with a long and painful rehabilitation and emotional trauma.
William Eklund, an employee of Boeing Inc., underwent hip replacement surgery in 2006. At some point following surgery. he began experiencing extreme hip pain and a persistent squeaking of the hip. He then found out that the M2a Magnum Metal-on-Metal Hip system from Biomet was failing and eventually underwent revision surgery in 2014 to remove and replace the device.
This lawsuit is different because it marks the first time a large international corporation has sued Zimmer Biomet on behalf of an employee.
In a March 31, 2017 ruling, Zimmer was ordered to pay more than $2 million to a New Mexico man for a defective hip implant with an “unreasonably dangerous design.”
Yesterday, a federal jury in Dallas, TX, awarded a record $1 billion verdict against Johnson & Johnson and its DePuy Orthopaedics unit to six plaintiffs injured by the company’s Pinnacle metal-on-metal hip implants.
More and more people turn to hip replacement surgeries to give them back their mobility and to relieve the pain caused by diseases such as osteoarthritis.
On November 1, 2016, under a Master Settlement Agreement (MSA), Wright Medical Technology, Inc., reached a $240 million settlement agreement for nearly 1,300 product liability lawsuits filed by individuals nationwide over its metal-on-metal hip implants.
Earlier this month, we updated you on a Hazard Alert regarding a taper lock failure for a specific range of LFIT-V40 Metal Heads.
Other serious problems have been reported related to the LFIT-V40 chrome/cobalt heads, which include:
Our knowledgeable staff is available at (877) 284-6600.
On September 27, 2016, the Therapeutic Goods Administration (TGA) in Australia, in consultation with Stryker Orthopaedics, issued a hazard alert for a specific range of LFIT Anatomic CoCr V40 femoral heads.
Medical device manufacturer Zimmer Biomet has issued a voluntary field safety corrective action for its M2a 38mm metal-on-metal hips warning European surgeons of problems with the device. Even though there are thousands of patients in the US with the same device, no such warnings have been issued here.
Joint replacement infections can develop while you’re still in the hospital or after you go home. There are many complaints from patients alleging their infections were caused during the actual joint replacement surgery itself when a forced-air warming unit commonly used by hospitals called the Bair Hugger was used.