Depuy Implant Recalls (Now a Subsidiary of Johnson and Johnson) This implant manufacturer was a part 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 numerous reports that the femoral head component was fracturing at a bigger rate than what was expected. Depuy Orthopedics was 1 of the eight manufacturers that issued recalls of their hip implant systems as a result of employing St. Gobain Desmarquestâ&euro&trades zirconia ceramic femoral heads in their joint replacement items.

In the late 1990s, Depuy withdrew its Hylamer Polyethylene Bearing Surface product from the marketplace. This item was initially 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 following a study showed that patients were showing a high failure rate for the device.

In 2008, Depuy issued one more recall on its LCS Knee â&euro&ldquo Orthopedic knee implant Meniscal bearing insert. This item is intended to replace a knee joint in order to relieve pain and restore function to the knee. The reason for the recall was that the product was not labeled effectively and mis-etched as to size. As a result of these recalls there may be Depuy hip implant lawsuits against the manufacturer.

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 successfully to the bone when implanted. This induced enhanced discomfort and loosened joints in patients with the knee implant systems. The failure of these knee implant goods led a quantity of patients to have additional surgeries to fix the dilemma. These additional surgeries resulted in longer rehabilitation instances for the patient and also heightened dangers for the duration of the operation.

In 2007, Smith & Nephew issued an additional recall after 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 yet another voluntary recall in January of 2008 of its TC-PLUS, VKS, and RT-PLUS item lines. The medical implant manufacturer was informed by a single of its suppliers that the semi-completed knee implant castings contained greater-than-specified iron content material. The merchandise becoming recalled had been manufactured by Smith & Nephew’s subsidiary, Plus Orthopedics.

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