Wounds can impact physical well-being and general health, often requiring surgical intervention. The knee joint, a delicate and crucial body component, can be affected by various injuries. The knee, the largest joint in the body, is vital for daily activities. However, the damage can’t be fully repaired, making patients often opt for knee replacement surgery to replace the joint with artificial components. Since 1968, knee replacement surgery has become common, primarily for elderly patients and athletes with physical stress. In 2021, the American Academy of Orthopaedic Surgeons reported 753,818 complete knee arthroplasties in the U.S.
Faulty medical devices can cause surgery complications, potentially resulting in implant manufacturer liability if patients don’t recover. This issue is common in knee joint replacement surgery. Exactech is the only US firm facing a knee replacement lawsuit, while Zimmer may face NexGen lawsuits in the UK due to numerous recalls of knee replacement devices. Exactech has recalled its defective knee implants since 2004, causing safety concerns and attracting FDA attention. The memory includes hip and ankle replacements. The packing flaw exposed the polyethene insert to oxygen, causing oxidation and degradation of knee replacement material, leading to early failure and potential health issues in medical device implants like Exactech, Inc.
Knee implant manufacturers must promote their products, warn patients about hazards, and address excessive sedentary behaviour, as 90% of patients post-surgery report significant weariness after five years. Manufacturers are responsible for checking their product’s post-FDA approval, but some argue the 510(k) process falls short of preventing dangerous effects. This allows manufacturers to demonstrate products equivalent to rival models, leading to lawsuits.
Patients with faulty Stryker knee replacements should consult their surgeon and a knee implant recall attorney for prompt consultation on device failure symptoms. Medical equipment malfunctions, causing injuries and causing damage. Manufacturers like Stryker issue recalls, but thousands of patients may still be at risk before removing the product. The increase in revision operations, potential injuries, and legal actions against businesses that failed to test their products or warn American consumers adequately is a result.
Medical devices like knee replacements can be recalled through three methods: voluntarily by producers, FDA-ordered by manufacturers, or forced by the FDA in severe cases or non-compliance with requests. The FDA may take legal action if a recall isn’t issued, as manufacturers usually conduct voluntary recalls or collaborate on recall requests. Most knee replacement recalls were voluntary or required due to FDA concerns resulting from adverse events or recognised issues in patients who received the devices.
An infection could occur even if a knee replacement is booming due to bacterial growth on or around the joint replacement components or if the prosthesis breaks down, causing further infection. Exactech’s knee replacements were impacted by improper packaging, exposing them to oxygen, leading to faster deterioration and revision surgery for many patients.
This article helps you understand the stryker knee replacement recall and what it involves.