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Michigan-Based Stryker Corp. and Its Howmedica Osteonics Subsidiary Are Targeted in Defective Hip Implant Lawsuit
Date:9/13/2013

Southfield, Michigan (PRWEB) September 13, 2013

Like thousands of other patients with debilitating hip pain, Arthur Curnow sought appropriate medical treatment, took his physician’s advice, and underwent two successive surgeries in 2010 to replace his right and left hips. Then things got worse.

According to court documents in a case recently filed in Macomb County Circuit Court (Number 2013-001999-NP), both hip implant devices – manufactured by Stryker Corporation and its wholly-owned subsidiary Howmedica Osteonics, and sold under “The Rejuvenate® System” product name – failed. Specifically, the metal surfaces in each device’s neck and stem began to rub against one another, causing metallic debris to shed, causing damage to the surrounding tissues. Blood tests revealed the presence of heavy metal ion contamination, and MRI results showed fluid collections around the hip implant. Eventually, his physician recommended revision surgeries to remove both Rejuvenate devices. At surgery, the damage caused by the metal debris was clearly visible.

“Both Mr. Curnow and his doctor trusted that Stryker and Howmedica had properly researched, tested, and marketed the Rejuvenate System,” says Robert B. Sickels, an attorney at Sommers Schwartz, P.C. who represents Arthur Curnow and his wife in a lawsuit recently filed in Macomb County Circuit Court (Case Number 2013-001999-NP). “As we now know from the recall of the product, Rejuvenate simply wasn’t safe and people were seriously injured.”

Approved for sale in the U.S. in 2008, the Rejuvenate device was implanted in an estimated 20,000 patients before Stryker issued a recall in July 2012 that also included its ABG II product, another modular stem design. Typically, hip implants are expected to last 15 to 20 years, but many Rejuvenate patients have suffered failures within two to five years after implantation.

“The most significant risk inherent in the Rejuven
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3. The FDA Issues Class 1 Recall for Stryker’s Oasys Midline Occiput Plate Due to a Key Defect, Reports Parker Waichman LLP
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