The U.S. Food and Drug Administration (FDA) has issued a Class I recall for a hip implant device manufactured by Chinese company MicroPort Orthopedics. According to the agency, it was found that the Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck, used in hip replacement systems, could fracture after implantation, leading to complications such as sudden pain, instability, and difficulty walking and performing ...
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