The Many Difficulties in Diagnosing Problems in Recipients of Stryker Rejuvenate Hip Implants

The Stryker Rejuvenate and ABGII hip implant systems were voluntarily recalled by the company in July of 2012. The recall cited potential fretting and corrosion at the neck juncture as the primary reason for the recall. New information, however, points to a different reason for the corrosion and possible metal ion release.
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Stryker Sales Slip Following Recall of Rejuvenate and ABGII Hip Implants

Stryker Orthopedics experienced a dip in its third-quarter sales, likely due to the recall of the Rejuvenate and ABGII in July of this year. While the sales of reconstructive joint implant systems dropped approximately one percent overall, Stryker’s hip implant sales dropped nearly 10 percent and its knee implant sales dropped 4.3 percent.
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New Jersey Sees Consolidation of Stryker Rejuvenate Hip Lawsuits

At least ten Stryker Rejuvenate and ABGII hip implant lawsuits are expected to be centralized in the State of New Jersey before one judge in order to coordinate the handling of the suits. Application for Multi-county Litigation has been made in hopes of consolidating all Rejuvenate and ABGII lawsuits.
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The Stryker Rejuvenate and Stryker ABGII Hip Implant Recalls

Stryker Orthopedics issued a recall in July of 2012 for their Rejuvenate and ABGII hip implants. This recall followed a May 2012 Canadian recall as well as an Urgent Safety alert sent out to hospitals and physicians in April, 2012 regarding the potential risks of these two hip implants.
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Stryker ABGII Hip Implant Revision Surgery: The Dangerous Potential Complications

Recipients of a Stryker Rejuvenate or ABGII Hip implant device may have been shocked to hear that both implants were recalled in July of 2012. Or, if you are one of the recipients who had already suffered adverse health effects from the Rejuvenate or ABGII then perhaps you were not so surprised to hear of the recall.
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