# China NMPA Product Recall - Disposable vacuum blood collection tubes

Source: https://www.globalkeysolutions.net/records/china_product_recall/jiangxi-sanxin-medical-technology-co-ltd/76f6b2e2-885e-4237-9f33-5b343887567a/
Source feed: China

> China NMPA product recall for Disposable vacuum blood collection tubes by Jiangxi Sanxin Medical Technology Co., Ltd. published August 30, 2019. Recall level: Level 3 Recall. Jiangxi Changqing Medical Technology Co., Ltd. initiated a voluntary Class III recall of its disposa

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Jiangxi Changqing Medical Technology Co., Ltd. has initiated a voluntary recall of disposable vacuum blood collection tubes.
- Company Name: Jiangxi Sanxin Medical Technology Co., Ltd.
- Publication Date: 2019-08-30
- Product Name: Disposable vacuum blood collection tubes
- Recall Level: Level 3 Recall
- Recall Reason: The presence of quality defects in disposable vacuum blood collection tubes affects test results.
- Discovering Company: Jiangxi Changqing Medical Technology Co., Ltd.
- Manufacturing Company: Jiangxi Sanxin Medical Technology Co., Ltd.
- Summary: Jiangxi Changqing Medical Technology Co., Ltd. initiated a voluntary Class III recall of its disposable vacuum blood collection tubes (Registration Certificate No.: Ganxiezhuzhun 20142410352) as announced by the National Medical Products Administration (NMPA) on August 30, 2019. This action was taken due to identified quality defects within these medical devices, which have the potential to compromise the accuracy of patient test results. While specific inspection dates were not detailed in this public announcement, the recall signifies the company's proactive response to address product quality concerns under the NMPA's regulatory oversight for medical devices in China. A Class III recall indicates that the use of, or exposure to, the affected product is not likely to cause adverse health consequences. The company is required to implement the recall by removing the defective products from the market. Comprehensive details regarding the specific models, specifications, and affected batches of the disposable vacuum blood collection tubes are available in the "Medical Device Recall Event Report Form." This document serves as the official record providing critical information for stakeholders to identify and manage the recalled items effectively, ensuring patient safety and product integrity. The NMPA, as the governing body, ensures that such recalls are conducted appropriately to protect public health.

Company: https://www.globalkeysolutions.net/companies/jiangxi-sanxin-medical-technology-co-ltd/947586e0-a6fe-4685-8279-bd6c8a0e4b4e/