Stryker Hip Replacement Recalls
Stryker issued recalls for hip implants due to fretting, corrosion, and other issues, leading to numerous lawsuits and the most extensive recalled products. Stryker recalled Trident PSL and Hemispherical Acetabular Cups in 2008 due to production issues, failing residue tests despite FDA warnings, and voluntarily withdrawing the products.
Recall processing with broad spire care management
Stryker contracted Broadspire Care Management to handle claims and data for the Rejuvenate and ABG II recall, covering patients’ out-of-pocket medical expenses, including revision surgeries. Before the Stryker recall, DePuy, a hip implant maker, partnered with Broadspire to manage patient claims for faulty implants. Under Broadspire’s agreement, insurance company doctors decided if an implant needed replacement. Critics fear Broadspire may use its position to obtain patient medical records, potentially using them against patients in court for defective implant cases, and raise privacy concerns.
Which Stryker hip implants have been recalled?
Stryker Howmedica Osteonics Corporation voluntarily recalled several artificial hip implant systems in 2012 due to patient complaints and safety concerns following a decade-long FDA investigation into using these implants.
Stryker recalled its Rejuvenate hip replacement system in April 2012 due to a reported rate of less than 1% of revisions potentially causing fretting or corrosion at the modular neck junction.
Stryker lfit anatomic V40
Stryker Accolade and LFIT Anatomic V40 Femoral Head hip replacement devices were recalled due to taper lock failure injuries. Over 42,000 units were identified from the U.S. and other countries, with affected patients notified.
What to do if you received a recalled hip replacement
Stryker Corporation advises patients with recalled devices to undergo revision hip replacement surgery. For artificial hips, consult with someone and consult a personal injury attorney for recording symptoms and preserving product liability claims against Stryker. Seek medical attention for discomfort or swelling around a hip replacement implant as soon as possible. Waiting too long may result in irreparable harm and loss of legal rights. Gather medical records and proof to demonstrate the severity of injuries from recalled implants.
Defective hip implant system layouts
Metal-on-metal hip implants pose health risks, requiring hip joint replacement surgery for many injured patients. Recalled Stryker hip implant systems require partial and total replacement units. Stryker, a company that plans to replace the acetabulum and femoral head of a patient’s native hip with tidal hip joint devices, has issued urgent recall warnings, highlighting potential metal ion generation, debris release, and metallosis.
Stryker Rejuvenate and ABG II problems
Stryker has launched a reimbursement programme for out-of-pocket costs related to ABG II and Rejuvenate diagnostics, covering all necessary expenses for patients without or without insurance. Stryker Rejuvenate and ABG II pose risks like metallosis, pseudotumors, oedema, necrosis, osteolysis, and severe pain. Firms should be held accountable for pain and suffering.
The Stryker knee replacement recalls are pretty intense, but this article tries to explain to you more about this, and when you decide to get one, you can have an overview of what to expect throughout the whole process.