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A patient who had an ABG II Modular Neck Hip Stem or Rejuvenate Modular Neck Hip Stem implanted, who underwent a subsequent surgery to have the hip implant removed prior to September 9, 2020 and within 10 years of implantation, and who otherwise meets the 2020 Settlement Program's eligibility requirements, will receive a Base Award under the ...
Stryker’s toll-free Patient Care Line can be reached by calling 1-888-317-0200 (U.S. and Canada only). The Patient Care Line is available from 8am–9pm EST, Monday through Saturday. Information about the Voluntary Recall. Stryker initiated a voluntary recall of its Rejuvenate Modular and ABG II modular-neck hip stems in June 2012.
However, corrosion, fretting loosening and the release of toxic metals were all reported. Stryker voluntarily recalled all of its Rejuvenate and ABG II hip replacements from the market in July 2012. The potential for fretting and corrosion that could cause pain, swelling and tissue damage prompted the recall.
From 2009 to 2013, the Stryker Corporation issued permanent recalls for two of the company’s hip replacement systems and multiple recalls for one of its hip stems. It recalled the Rejuvenate and ABG II hip implants in 2012, halting all global sales and production of the components. The recall came three months after Stryker issued an urgent ...
2. Have had an ABG II Modular Neck Hip Stem and/or Rejuvenate Modular Neck Hip Stem implanted in the United States (or at any United States Military Hospital); 3. Have undergone a surgery to remove the implanted modular-neck hip stem for reasons related to the recall at least 181 days after implantation , prior to September 9 , 2020, within 10 ...
The Synovo Total Hip System is also referred to as the Total Hip Replacement System, and also as Synovo Preserve and Endotec BP. Recommendations for Patients Who May Have Received these Devices ...
In one of the largest national landmark settlements, the global medical devices and equipment manufacturing company, Stryker Corp., will pay out $1.43 billion to patients who had hip implant revision surgery to remove defective Rejuvenate or ABG II Modular-Neck Hip Stems. It is imperative for any victim who suffers serious injury or illness from the…
The first recall of Stryker hip implants involved two of the company’s products: Rejuvenate and ABG II modular-neck stems. The recall was announced in June 2012. Years later, on November 9, 2016, the FDA announced a recall of Stryker LFIT V40 Femoral Heads (metal Cobalt Chrome heads) manufactured as early as 2006.
The previous master settlement in the Stryker Hip Implant Recall [MDL 2441] does not cover patients that have surgery or testing after November 3, 2014. This claim must be made timely and within the statute of limitations of the resident state of the affected patient. Time is of the essence.
Claims Administration Procedure No. 2 (October 26, 2016) – Abductor Repair. Claims Administration Procedure No. 3 (November 11, 2016) – Re-Revision Surgery (Revision of Proximal Body Only) Claims Administration Procedure No. 4 (November 11, 2016) – Intra-Operative Femur Fracture Without Osteotomy. The above document (s) are in PDF format.