# China NMPA Product Recall - CS600 MSN Anesthesia System

Source: https://www.globalkeysolutions.net/records/china_product_recall/ge-healthcare-systems-trade-development-shanghai-co-ltd/f3283b85-0ba3-427e-99a2-2e2d69d34ff6/
Source feed: China

> China NMPA product recall for CS600 MSN Anesthesia System by GE Healthcare Systems Trade Development (Shanghai) Co., Ltd. published December 23, 2019. Recall level: Level 2. On December 23, 2019, the National Medical Products Administration (NMPA) announced a voluntary reca

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. is voluntarily recalling the CS600 MSN anesthesia system.
- Company Name: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Publication Date: 2019-12-23
- Product Name: CS600 MSN Anesthesia System
- Recall Level: Level 2
- Recall Reason: Cable connections may become loose in some batches of products, which could prevent the mechanical ventilation function from working.
- Discovering Company: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Manufacturing Company: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Summary: On December 23, 2019, the National Medical Products Administration (NMPA) announced a voluntary recall initiated by GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. The recall impacts their CS600 MSN Anesthesia System, registered under certificate number 国械注进 20183540068. The company identified a critical issue in certain product batches: potentially loose cable connections. This defect could lead to the inability to use the mechanical ventilation function, raising significant patient safety concerns. In response, GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. has implemented a Class II recall. This classification signifies that the use of, or exposure to, the affected product may cause temporary or medically reversible adverse health consequences, or that the probability of serious adverse health consequences is remote. The company committed to providing specific details on affected models, specifications, and batch numbers via a "Medical Device Recall Event Report Form" to ensure efficient management of the recall and resolution of the product deficiency.

Company: https://www.globalkeysolutions.net/companies/ge-healthcare-systems-trade-development-shanghai-co-ltd/4d6c1bd7-e2c1-400d-b03c-385df7470df5/