# 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/d0d58879-6a15-4bdc-9960-65bbe169d138/
Source feed: China

> China NMPA product recall for Mobile C-arm X-ray machine by GE Healthcare Systems Trade Development (Shanghai) Co., Ltd. published July 19, 2021. Recall level: Level 2 Recall. GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. has announced a voluntary Class II re

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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: 2021-07-19
- Product Name: Mobile C-arm X-ray machine
- Recall Level: Level 2 Recall
- Recall Reason: The issue concerns the potential premature depletion of button batteries in OEC Elite systems manufactured after January 2019.
- 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. has announced a voluntary Class II recall concerning its mobile C-arm X-ray machines. The recall, published on July 19, 2021, by the Shanghai Municipal Drug Administration and overseen by the National Medical Products Administration (NMPA), addresses a significant performance issue. Specifically, OEC Elite systems manufactured after January 2019 have exhibited premature battery depletion, which could potentially affect the operational reliability and availability of these essential medical imaging devices during clinical use. The company proactively initiated this recall to ensure the safety and effectiveness of its products, aligning with stringent medical device regulations. A Class II recall signifies that the use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. Comprehensive details regarding the exact models, specifications, and affected production batches are provided in the accompanying "Medical Device Recall Event Report Form." This action highlights the manufacturer's commitment to product quality and patient safety within the regulatory framework established by the NMPA.

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