# China NMPA Product Recall - Mobile C-arm digital X-ray system, Series 9800 mobile C-arm, mobile C-arm X-ray machine

Source: https://www.globalkeysolutions.net/records/china_product_recall/ge-oec-medical-systems-inc/e7e254b3-d3e1-485e-b38f-35b4f86f9ed6
Source feed: China

> China NMPA product recall for Mobile C-arm digital X-ray system, Series 9800 mobile C-arm, mobile C-arm X-ray machine by GE OEC Medical Systems, Inc. published January 13, 2017. Recall level: . On December 23, 2016, GE OEC Medical Systems, Inc. initiated a voluntary recall, reported to the Nat

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: GE OEC Medical Systems, Inc. is recalling products including mobile C-arm digital X-ray systems.
- Company Name: GE OEC Medical Systems, Inc.
- Publication Date: 2017-01-13
- Product Name: Mobile C-arm digital X-ray system, Series 9800 mobile C-arm, mobile C-arm X-ray machine
- Recall Reason: Random failures in the workstation power cord can cause loss of image functionality. To date, no injuries have been reported due to this failure. Nevertheless, the failure could potentially lead to surgical interruption, requiring additional medical intervention.
- Discovering Company: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Manufacturing Company: GE OEC Medical Systems, Inc.
- Summary: On December 23, 2016, GE OEC Medical Systems, Inc. initiated a voluntary recall, reported to the National Medical Products Administration (NMPA) by its Chinese distributor, GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. The recall pertained to several mobile C-arm digital X-ray systems, including models MiniView 6800, Series 9800, and OEC 9900 Elite. The core issue identified was random power cord failures in the workstation, which could result in the loss of image functionality during procedures. While no injuries were reported, this malfunction posed a risk of surgical interruption, potentially necessitating additional medical intervention.
Operating under the NMPA's regulatory oversight, the company confirmed that the specific affected batches of products were not sold or imported into China. This was attributed to differences in power cord specifications required for the Chinese market. Consequently, the primary action within China involved the NMPA requesting provincial food and drug administration departments to enhance their supervision and management over similar medical devices. Chinese consumers or medical facilities were advised to contact GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. with any inquiries, reinforcing that the direct impact of this recall was limited to regions like the USA and Canada.

Company: https://www.globalkeysolutions.net/companies/ge-oec-medical-systems-inc/6ef83ead-6c29-4473-b97d-60bc22e65183