Medtronic Inc. Initiates Class III Voluntary Recall of Medtronic Evolut PRO+ Transcatheter Aortic Valve System Due to Regulatory Compliance Issues in Thailand

Medtronic (Shanghai) Management Co., Ltd. reported that due to regulatory compliance issues with the product in Thailand, the manufacturer, Medtronic Inc., initiated a voluntary recall of its Transcatheter Aortic Valve System, Medtronic Evolut PRO+ System (Registration No.: 20243130221). The recall is classified as a Level Three Recall. The products involved in this recall were not imported into China. For specific model, specifications, batch numbers, and other detailed information, please refer to the "Medical Device Recall Event Report."