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Stryker Rejuvenate Orthopaedics Product Recall

Phillips Law Firm can help with your Stryker Hip Recall Claim


Glenn Phillips Stryker RecallHip implant products "Rejuvenate" and "ABG II" by medical manufacturer Stryker Orthopaedics (also known as Howmedica Osteonics) have now been recalled. An astounding number of patients have undergone hip joint surgery only to discover that they need to have the defective product removed and replaced with additional arthroplasty. If you are a victim of one of these defective products, contact Phillips Law Firm immediately. Our experienced attorneys help protect your rights and seek justice on your behalf. Don't let the statute of limitations interfere with your right to compensation for your suffering, it is important to contact us now!

stryker hip orthopedics recall

Which Stryker products are being recalled?

The "Rejuvenate" and "ABG II" are modular-neck stems used during hip arthroplasty that were voluntarily recalled in August 2012 by the manufacturer Stryker Orthopaedics. While the manufacturer is New Jersey based, more and more victims are coming forward nationally.

What are the side effects of the "Rejuvenate" and "ABG II" hip implants?

stryker hip implant recallScientific evidence concludes that the metal stem in models "Rejuvenate" and "ABG II" are susceptible to corroding and fretting which can lead to metal ion deposits in the surrounding soft tissue. The products are not metal-on-metal devices like the recalled Johnson & Johnson's DePuy ASR product however they still pose a risk for metal ion build up. The increased levels of chromium ions and cobalt in the bloodstream can be a toxic combination leading to adverse reactions. The adverse reactions include bone dissolution, pseudo tumors, necrosis (death) of skin tissue, bone and muscle and inflammation of the synovial membrane which are all issues that can cause additional bodily harm, pain, swelling and further health complications. Get compensation for your suffering!

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Phillips Law News

If you have received a "Rejuvenate" or "ABG II" hip implant it is important to note that the recall is an urgent safety alert from the FDA. You can find out which stem part of your hip implant product was used during your surgery by contacting your surgeon. It may be a possibility that your surgery has included "Rejuvenate" product because the line has been on the market since its approval in 2008. If you find that the "Rejuvenate" or "ABG II" was used during your surgical process contact Phillips Law Firm immediately. We are waiting 24/7 to answer any questions you may have and discuss your options with a free case consultation.

How serious is the Stryker hip implant product recall?

Hip arthroplasty can be a painful surgical process the first time, and the additional required revisional surgery to remove and replace the defective product can be a painful and costly process requiring a long recovery time. Our attorneys will seek compensation for your past, current and future pain, suffering, and medical expenses. We empathize with you and understand the traumatic and unfortunate experience you have undergone and want to help. We will take care of your legal matters while you heal.

Call Phillips Law Firm today!

Don't wait; call us today (800) 708-6000 to get the justice you deserve. Remember that we have a "no fee promise" meaning if we do not recover compensation for you, you do not owe us a dime. Phillips Law Firm has the positive, case-winning reputation you are seeking. Let us help you, get started today.


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