Stryker Rejuvenate Hip Patients: What Should You Do If You Have a Recalled Hip But No Pain?

Many recipients of the Stryker Rejuvenate hip implant have been dismayed to find they may have the same sort of serious health issues as recipients of metal-on-metal implants. The Rejuvenate was recalled in July of 2012 with Stryker stating there was the risk of fretting and corrosion at the neck juncture.
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Why am I in Pain from my Stryker Rejuvenate Hip Implant and What are My Options?

Unfortunately for many recipients of the Stryker Rejuvenate hip implant who are suffering chronic and severe pain, there is no way to stop this pain other than a risky and painful revision surgery. Although not all Stryker implant recipients will experience pain, those that do have likely suffered tissue necrosis resulting from corrosion or fretting of the device.
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Chromium and Cobalt Poisoning from the Stryker Rejuvenate Hip

Any patient with a Stryker Rejuvenate hip implant should be aware of the potential risks involved, particularly those associated with cobalt and chromium poisoning. Rejuvenate recipients should take care to have their blood checked for levels of chromium and cobalt in order to determine whether fretting or corrosion has occurred.
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The DePuy ASR Hip: Status of the Litigation

The DePuy ASR hip implant, approved by the FDA in 2005 and recalled in August, 2010 has had over 6,000 lawsuits filed against DePuy and parent company Johnson & Johnson. For states which operate under a two-year statute of limitations, that SOL ran this past August.
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The DePuy ASR Hip: Even if You Have No Pain, You Should Consult With an Attorney

The DePuy ASR hip implant was approved by the FDA in 2005, yet a mere five years later, in August of 2010, the device was recalled. The ASR gained approval through the FDA’s 510(k) process based on the device being substantially equivalent to DePuy’s Pinnacle hip implant. While the ASR is an all-metal hip implant device, the Pinnacle includes ceramic and polyethylene models as well.
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