# China NMPA Product Recall - Mobile C-arm X-ray machine

Source: https://www.globalkeysolutions.net/records/china_product_recall/ge-healthcare-systems-trade-development-shanghai-co-ltd/68ceacc2-9bc3-4625-a225-7c77aefa5667/
Source feed: China

> China NMPA product recall for Mobile C-arm X-ray machine by GE Healthcare Systems Trade Development (Shanghai) Co., Ltd. published August 06, 2019. Recall level: Level 2. GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. voluntarily initiated a Class II reca

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. is voluntarily recalling its mobile C-arm X-ray machine.
- Company Name: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Publication Date: 2019-08-06
- Product Name: Mobile C-arm X-ray machine
- Recall Level: Level 2
- Recall Reason: A system board in some batches of products may fail. If this failure occurs, imaging functionality will be lost. This could lead to treatment delays or changes in medical plans.
- Discovering Company: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Manufacturing Company: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Summary: GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. voluntarily initiated a Class II recall of its mobile C-arm X-ray machines, as announced by the National Medical Products Administration (NMPA) on August 6, 2019. This proactive measure addresses a critical technical issue where a system board in certain product batches may malfunction. The primary concern is the potential loss of imaging functionality, which could lead to significant treatment delays for patients or necessitate alterations to their medical plans, directly impacting healthcare delivery. This recall falls under the regulatory purview of the NMPA and the Shanghai Food and Drug Administration, underscoring compliance with Chinese medical device regulations. While no specific inspection dates were provided, the company itself reported the defect. The affected devices are identifiable by Registration Certificate No.: 20163304728. The required action for GE Healthcare involves a comprehensive identification and recall of all impacted product models, specifications, and batches, with further details available in the "Medical Device Recall Event Report Form," to ensure effective mitigation of patient risks.

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