Stryker Hip Lawsuit

The neck components of the rejuvenate and abg ii are made of chromium and cobalt and the stems are coated with titanium. Stryker s products have continued to pose dangers to orthopaedic patients. In 2016 stryker issued a recall for their v40 femoral head products which are the metal ball portions of hip replacements that work with hip stems like the accolade tmzf and accolade 2 to replicate the movement of hip joints.

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The metals can cause tissue damage loosening of the implants and other complications.

Stryker hip lawsuit.

Stryker hip replacement v40 femoral head recall. Stryker hip lawsuits claim faulty hip implants caused severe pain and other complications that required additional surgery to repair. Stryker s official recall announcement dated july 6 2012 stated that the company decided to recall the hip replacements when it received the disturbing data. Patients who had surgery to replace their rejuvenate.

Stryker hip lawsuit alert expert legal help available for those suffering hip implant side effects. Stryker orthopaedics and court appointed committees of attorneys representing rejuvenate modular neck hip stem and abg ii modular neck hip stem plaintiffs in new jersey multicounty and federal multidistrict litigations reached an agreement to compensate certain additional eligible u s. Attorneys are investigating possible stryker accolade lawsuits alleging patients were harmed by defective hip implants although stryker accolade has reportedly been linked to an increased risk of. Stryker has already recalled several hip implant models including the trident rejuvenate abg ii and accolade tmzf.

Thousands of stryker hip lawsuits have been filed against stryker orthopaedics for injuries caused by its implant devices including rejuvenate abg ii and lfit v40 femoral head. Stryker hip devices may have caused serious side effects and injuries including metallosis implant failure and required revision surgery. In its recall notice stryker said the artificial hip systems pose a risk of fretting and or corrosion at or around the modular neck junction. Stryker orthopaedics announced in july 2012 that it was recalling its rejuvenate modular and abg ii modular neck hip stem implant devices.

The initial settlement agreement was later amended in july 2015 and then again in december 2016 which expanded the number of. They have now issued a warning and recall for certain lfit v40 femoral heads used on the accolade tmzf accolade 2 meridian and citation hip implant stems. Each year more than 225 000 people undergo hip replacement surgery in the united states. The lawsuits blame metal parts in the implants for releasing toxic metal ions into the body.

In december 2014 stryker offered 1 425 billion to settle more than 5 000 lawsuits related to rejuvenate and abg ii modular neck hip implants which were made and sold by the company s howmedica osteonics subsidiary. Many of these are performed with popular brands such as the stryker rejuvenate and abg ii implant systems.

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