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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.
Stryker hip lawsuit. Patients who had surgery to replace their rejuvenate. 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. The lawsuits blame metal parts in the implants for releasing toxic metal ions into the body. 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 hip lawsuits claim faulty hip implants caused severe pain and other complications that required additional surgery to repair. The metals can cause tissue damage loosening of the implants and other complications. Stryker hip devices may have caused serious side effects and injuries including metallosis implant failure and required revision surgery. Stryker has already recalled several hip implant models including the trident rejuvenate abg ii and accolade tmzf.
Stryker orthopaedics announced in july 2012 that it was recalling its rejuvenate modular and abg ii modular neck hip stem implant devices. 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 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. Stryker hip replacement v40 femoral head recall.
The neck components of the rejuvenate and abg ii are made of chromium and cobalt and the stems are coated with titanium. Many of these are performed with popular brands such as the stryker rejuvenate and abg ii implant systems. 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. 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.
The initial settlement agreement was later amended in july 2015 and then again in december 2016 which expanded the number of. Stryker s products have continued to pose dangers to orthopaedic patients.
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