# China NMPA Product Recall - treadmill

Source: https://www.globalkeysolutions.net/records/china_product_recall/ge-healthcare-systems-trade-development-shanghai-co-ltd/e76adb1e-50b5-4813-b92f-733307342635
Source feed: China

> China NMPA product recall for treadmill by GE Healthcare Systems Trade Development (Shanghai) Co., Ltd. published July 23, 2019. Recall level: Level 3 Recall. GE Healthcare Systems Trading Development (Shanghai) Co., Ltd. initiated a voluntary Class III recal

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd. has initiated a voluntary recall of the runway.
- Company Name: GE Healthcare Systems Trade Development (Shanghai) Co., Ltd.
- Publication Date: 2019-07-23
- Product Name: treadmill
- Recall Level: Level 3 Recall
- Recall Reason: Some batches of GE T2100 treadmills sold to customers had incorrect registration certificate numbers.
- 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. initiated a voluntary Class III recall of specific batches of its GE T2100 treadmills, as reported on July 23, 2019. This action was prompted by the discovery of incorrect registration certificate numbers associated with some of the treadmills sold to customers. The affected products were identified as having Registration Certificate No.: ". The recall was reported through the Shanghai Food and Drug Administration Medical Device Recall 2019-167, operating under the oversight of the National Medical Products Administration (NMPA). The company voluntarily took responsibility to address this discrepancy, emphasizing its commitment to regulatory compliance and product accuracy. A Class III recall indicates that the use of, or exposure to, a violative product is not likely to cause adverse health consequences. Detailed information regarding the models, specifications, and batches involved in this recall is available in the 'Medical Device Recall Event Report Form' provided by the NMPA. This proactive measure by GE Healthcare Systems Trading Development aims to rectify the administrative error and ensure that all product information aligns with regulatory standards.

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