China NMPA Product Recall - Disposable infusion pump

Nanchang Beoite Medical Technology Co., Ltd. initiated a voluntary Class III recall of its disposable infusion pumps (Registration Certificate No. 20163542464). The company reported this action to the National Medical Products Administration (NMPA) on September 30, 2019. The primary reason for the recall was identified as non-compliance with standard requirements for the medical devices. While no specific inspection dates are provided, the recall itself is a proactive measure taken by Nanchang Beoite Medical Technology Co., Ltd. under the oversight of the NMPA, which governs medical device safety and quality in China. This voluntary recall aims to address the identified issues and ensure product safety. Detailed information regarding the specific models, specifications, and affected batches of the disposable infusion pumps is contained within the