FDA Class 1 Recall for MicroPort Hip Replacement Device
Serious Hip Replacement Device Recall. The Food and Drug Administration (FDA) has assigned its most serious device recall designation to the recall of China's MicroPort replacement hip joint. The MicroPort Orthopedics' Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck device is under Class 1 recall because … [Read more...] about FDA Class 1 Recall for MicroPort Hip Replacement Device
MicroPort Hip Replacement Device Under FDA Class 1 Recall
The MicroPort Orthopedics' Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck device is under Class 1 recall from the Food and Drug Administration (FDA). The FDA has assigned Class 1—its most serious device recall designation—to the recall of the MicroPort replacement hip joint, FierceMedicalDevices reports. MicroPort … [Read more...] about MicroPort Hip Replacement Device Under FDA Class 1 Recall
