The Food and Drug Administration (FDA) has ordered all producers of “metal-on-metal” artificial hips to undertake studies tied to high early failure rates and major negative health effects.
According to several media reports, the producers of “metal-on-metal” hips are required to conduct studies of patients to determine whether the implants are shedding high levels of metallic debris. The FDA sent the request to J&J and 20 other device makers, including Biomet Inc., Stryker Corp. and Zimmer Holdings Inc., asking them to conduct post-market surveillance of the hip replacements. Metal-on-metal hips, in which the ball-and-socket components are made from metals like cobalt and chromium, accounted for about one-third of the 250,000 hip replacement procedures preformed annually in the United States. (WCxKit)
The British Orthopedic Association, stated that one model of all-metal hip made by a unit of Johnson & Johnson was projected to not work in one-half of the patients who received it within six years after implant. The company no longer sells the ASR device. The British medical group also estimated, based on hospital data that the early failure rate for all-metal hips made by other manufacturers was higher than expected, ranging from 12% to 15% within five years after implant. Artificial hips are designed to last for 15 years or more.
According to Dr. Maisel, FDA. official, it was up to each manufacturer to determine how to conduct its studies. Under the agency rule, producers have 30 days to file a proposed plan with the FDA. He also indicated companies would be expected to collect information from patients who received the devices, including taking blood samples to determine the levels of metallic ion in their systems. The companies are also being asked to figure out how often the devices are not working. (WCxKit)
Along with the DePuy division of Johnson & Johnson, other major producers of hip implants include Zimmer, Stryker, Biomet and Wright Medical.
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