Stryker Hip Metallosis

May 03, 2016 - If you are the recipient of a Stryker Rejuvenate or Stryker ABGII hip implant device, you are likely aware of the recall issued in July 2012 as well as the Stryker hip settlement agreement offered to those who have undergone Stryker hip revision surgery. There are many issues associated with these Stryker devices, including Stryker hip corrosion and fretting, Stryker hip infection, Stryker hip blood poisoning and Stryker hip metallosis...
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Update on Wyoming Stryker Hip Litigation

Update on Wyoming Stryker Hip Litigation

The Stryker Rejuvenate/ABGII Hip Recalls and Subsequent Lawsuits

In July, 2012, Stryker Corporation issued a recall for the Rejuvenate and ABGII hip implants. These devices had been on the market barely more than two years at the time of the recall. When Stryker marketed the implants, they claimed the devices would be perfect for the younger, more active patient. The design of the two Stryker implants was extremely unique, in that there were a variety of stem and neck pieces in different lengths and angles, allowing surgeons to custom-fit the device to the patient according to body size, gender and level of activity. The design also implemented a ceramic, rather than a metal ball, which Stryker claimed made it much safer than other metal-on-metal hip implants, and less likely to shed cobalt and chromium metal ion debris due to Stryker Rejuvenate/ABGII fretting and corrosion. 

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Update on Wisconsin Stryker Hip Litigation

Update on Wisconsin Stryker Hip Litigation

The Status of the Stryker Rejuvenate/ABGII Hip Lawsuits

If your are the recipient of a Stryker Rejuvenate/ABGII hip implant, you likely heard of the Stryker Rejuvenate/ABGII hip recalls in July, 2012. Despite the fact that Stryker had marketed both devices as being safer than other metal-on-metal hip implants (due to the use of a ceramic ball) and much longer lasting that most all other hip implants, these claims turned out to be less than accurate. Shortly after the two devices were released in early 2010, adverse event reports began coming in to the FDA. These adverse event reports came from consumers and surgeons alike. In fact, several surgeons notified the FDA that they noted a substance which looked like “black rust” on Stryker Rejuvenate/ABGII hip implants removed from their patients. 

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What are the Short & Long Term Effects of Stryker Rejuvenate Chromium and Cobalt Exposure?

April 21, 2016 - Chromium Poisoning Resulting from a Stryker Rejuvenate Hip Device - Although many of the symptoms for chromium and cobalt poisoning are the same, there are some differences. Chromium VI is found in such things as automotive parts, stainless steel and medical implants, while Chromium III is used in microscopic amounts as a dietary supplement. The body attempts, through the liver and kidneys, to rid itself of toxic amounts of chromium...

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Update on West Virginia Stryker Hip Litigation

Update on West Virginia Stryker Hip Litigation

Should You File a West Virginia Stryker Rejuvenate/ABGII Hip Lawsuit?

Following the July, 2012 Stryker Rejuvenate/ABGII hip recalls, many injured consumers began coming forward to hold the company responsible for their injuries accountable. In December, 2013, four of six lawsuits chosen to undergo mediation were settled, and later in 2014, another 13 Stryker cases were settled. The judge in these cases wanted to determine whether some of the Stryker Rejuvenate/ABGII hip lawsuits could be settled prior to choosing bellwether cases which would represent larger groups of Stryker Plaintiffs. 

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