<p><img src="http://cdn.medgadget.com/img/Hip_implant_smithnephew.jpg" alt="" /></p> <p>Depuy Implant Recalls (Now a Subsidiary of Johnson and Johnson) This implant manufacturer was a element of the 2001 recall of zirconia ceramic femoral heads manufactured by St. Gobain Desmarquest. The recall was mandated by the Food and Drug Administration after many reports that the femoral head component was fracturing at a larger rate than what was expected. Depuy Orthopedics was one particular of the eight producers that issued recalls of their hip implant systems as a result of using St. Gobain Desmarquestâ&euro&trades zirconia ceramic femoral heads in their joint replacement goods.</p> <p>In the late 1990s, Depuy withdrew its Hylamer Polyethylene Bearing Surface item from the market. This item was originally developed to decrease wear in join implant components for the hip, shoulders, knees, and elbows. In 2001, the British governmentâ&euro&trades Medical Devices Agency issued a recall of knee implant Hylamer liners sterilized with gamma radiation in air. The recall was conducted soon after a study showed that patients had been showing a high failure rate for the device.</p> <p>In 2008, Depuy issued one more recall on its LCS Knee â&euro&ldquo Orthopedic knee implant Meniscal bearing insert. This product is intended to replace a knee joint in order to relieve discomfort and restore function to the knee. The cause for the recall was that the item was not labeled correctly and mis-etched as to size. As a result of these recalls there may be Depuy hip implant lawsuits against the manufacturer. </p> <p>Smith & Nephew Implant Recalls
This London based medical device manufacturer issued a recall of its Genesis II and Profix II Knee Implants to the Food and Drug Administration in 2003. The recall was a result of the failure of the knee implant systems to bond properly to the bone when implanted. This brought on elevated discomfort and loosened joints in patients with the knee implant systems. The failure of these knee implant merchandise led a number of patients to have additional surgeries to fix the dilemma. These further surgeries resulted in longer rehabilitation instances for the patient and also heightened risks all through the operation.
In 2007, Smith & Nephew issued another recall appropriate following a subscontractor incorrectly packaged the medical manufacturerâ&euro&trades BIRMINGHAM Hip Resurfacing Technique implants. As a result of the subcontractor error, diverse sizes of acetabular cups had been packaged together. It is evident people may want to file a hip implant lawsuit due to this error.
Smith & Nephew began an additional voluntary recall in January of 2008 of its TC-PLUS, VKS, and RT-PLUS product lines. The medical implant manufacturer was informed by a single distinct of its suppliers that the semi-finished knee implant castings contained higher-than-specified iron content material material. The goods becoming recalled were manufactured by Smith & Nephew's subsidiary, Plus Orthopedics.</p>
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