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MCS, Novation and Acumatch Hip Implants Recalled Due to Premature Deterioration

03/17/2022
Defective Medical Devices
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  Exactech, Inc., a medical device manufacturer headquartered in Gainesville, has recalled nearly 90,000 hip implant devices due to concerns of premature deterioration. The recall—which applies to the company’s MCS, Novation and Acumatch hip implant devices containing the company’s Connexion GXL liner—comes after two independent studies concluded that the synthetic […]

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Exactech, Inc. Recalls Connexion GXL Hip Implant Liners Over Safety Concerns

10/19/2021
Defective Medical Devices
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Exactech, Inc. is the manufacturer of acetabular polyethylene hip liner components that are used in certain hip implant systems. On June 28, 2021, Exactech, Inc. issued “Urgent Medical Device Correction” letters to agents, representatives, and distributors in possession of Exactech Connexion GXL polyethylene liners According to the United States Food […]

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Attorney Cal Warriner, with Searcy Denney Scarola Barnhart & Shipley, has negotiated his second national settlement program for the Stryker Rejuvenate and ABG II hip implant litigation

12/19/2016
Firm News
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Stryker Orthopaedics to compensate additional eligible U.S. patients who had surgery to replace their Rejuvenate Modular-Neck and/or ABG II Modular-Neck Hip Stems Kalamazoo, Michigan – December 19, 2016 – Stryker Corporation (NYSE:SYK) announced that Howmedica Osteonics Corp. (referred to as “Stryker Orthopaedics”), a subsidiary of Stryker Corporation, and Court-appointed committees […]

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Stryker Enters Settlement and Will Pay $1.43B to Settle Hip Implant Cases

11/4/2014
Mass Tort News
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Howmedica Osteonics Corp. (“Stryker Orthopaedics”), a subsidiary of Stryker Corporation, and Court-appointed committees of attorneys representing Rejuvenate Modular-Neck and ABG II Modular-Neck plaintiffs in New Jersey Multicounty and Federal Multidistrict litigations announced a Settlement Agreement. The lawsuits stem from two hip implants that Stryker recalled due to corrosion and other […]

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FDA Orders Investigation of Metal-on-Metal Hip Implants

09/17/2013
Do You Know?
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On May 6, 2011 the FDA ordered twenty-one artificial hip manufacturers to conduct an extensive investigation into whether the devices cause heavy metal poisoning in patients who receive them. Following up on medical reports of excessive levels of cobalt and chromium found in patients who received a particular type of […]

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Study: Women Suffer More Hip Implant Complications

02/22/2013
Articles
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In one of the largest studies of its kind, researchers have determined that women have a slightly elevated chance of needing a hip revision before a man. Researchers from Kaiser Permanente looked at 35,000 hip surgeries in 46 hospitals within their healthcare system. While men had an average of 1.9 […]

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