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
Recently Approved Medtronic Heart Valve Device under Class 1 Recall
Heart Valve Device Under Class 1 Recall. A component Medtronic's CoreValve Evolut R heart valve device is under Class 1 recall less than two months after receiving Food and Drug Administration (FDA) approval. The recall of the EnVeo R loading system has been designated a Class 1 recall, which is the FDA's most serious … [Read more...] about Recently Approved Medtronic Heart Valve Device under Class 1 Recall
